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The California Families Project (CFP) is an ongoing longitudinal study of Mexican origin families in Northern California. This study uses community, school, family, and individual characteristics to examine developmental pathways that increase risk for and resilience to drug use in Mexican-origin youth. This study also examines the impact that economic disadvantage and cultural traditions have in Mexican-origin youth. The CFP includes a community-based sample of 674 families and children of Mexican origin living in Northern California, and includes annual assessments of parents and children. Participants with Mexican surnames were drawn at random from school rosters of students during the 2006-2007 and 2007-2008 school year. Data collection included multi-method assessments of a broad range of psychological, familial, scholastic, cultural, and neighborhood factors. Initiation of the research at age 10 was designed to assess the focal children before the onset of Alcohol, Tobacco, and Other Drug (ATOD) use, thus enabling the evaluation of how hypothesized risk and resilience mechanisms operate to exacerbate early onset during adolescence or help prevent its occurrence. This study includes a diversity of families that represent a wide range of incomes, education, family history, and family structures, including two-parent and single-parent families.

The accompanying data file consists of 674 family cases with each case representing a focal child and at least one parent (Two-parent: n=549, 82 percent; Single-parent: n=125, 18 percent). Of the 3,139 total variables, 839 pertain to the focal child, 1,376 correspond to the mother, and 908 items pertain to the father.

Please note: While the California Families Project is a longitudinal study, only the baseline data are currently available in this data collection.

This study is part of the Seek, Test, Treat and Retain (STTR) Collaboration Project that involved over twenty studies in the fields of HIV and drug abuse. All studies were independently developed, but were chosen for the collaboration because they focused on one or more steps of the HIV treatment cascade: Seek, Test, Treat and Retain. As part of STTR Collaboration Project, the studies were grouped into Criminal Justice-related studies and Vulnerable Population-related studies. The data collected by these studies included twelve common domains (e.g., Demographic characteristics, Mental Health) in each of which a shared questionnaire or instrument was taken up by the studies and adapted to fit the study.

The main project of the CARE+ Corrections study is in Washington DC and is a RCT evaluating the "CARE+ Corrections intervention (a computerized tool integrating HIV treatment counseling, secondary transmission risk reduction counseling, and facilitated linkage to care through text message reminders)" versus standard of care among returning citizens in Washington, DC. The study is recruiting 100 participants who are incarcerated or were released from a correctional facility less than 6 months ago.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the August 2006 basic CPS questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in May 2006 (ICPSR 24781) and January 2007 (ICPSR 24783). These three supplements comprise the 2006-2007 waves of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

The TUS, like most CPS supplements, was designed to be a proxy response supplement, meaning a single respondent could provide answers for all eligible household members, provided the respondent was a household member 15 years of age or older. Unique to the TUS design were also a set of self-respondent supplement questions. All household members age 15 years and older who had completed the basic CPS core items were eligible for the August 2006 supplement items. Beginning in August 2006, 15-17 year old respondents were phased out of the TUS and they were entirely omitted from the January 2007 sample due to Census Bureau budget constraints.

The TUS consisted of items PEA1 through SINTTP. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for certain items. Information was collected from proxies on topics such as smoking status (items PEA1-PEA3) and the use of other tobacco-related products, such as pipes, cigars, chewing tobacco, and snuff (items PEAJ1A1-PEAJ1A4 and PEJ2A1-PEJSA4).

In addition to these smoking and other tobacco use status questions, self-respondents were queried on the following topics depending on their smoking/tobacco use status (i.e., every day, some days, or former cigarette smokers and/or users of other non-cigarette tobacco products):

• Smoking history

• Current cigarette smoking prevalence and consumption

• Type of cigarettes smoked

• Price of last pack/carton of cigarettes purchased and state of purchase

• Medical and dental advice to quit smoking

• Attempts and intentions to quit smoking cigarettes and/or other forms of tobacco use

• Awareness of 1-800-QUIT-NOW

• Workplace smoking policies and smoking rules in the home

• Attitudes toward smoking in public places

Another generally unique feature to the 2006-2007 TUS-CPS was the administration of questions to former smokers on their previous level of addiction, use of quitlines, and advice from health professionals. This feature enables comparisons between characteristics of former smokers (or successful quitters) and current smokers attempting to quit.

Demographic information collected include age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the February 2002 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in June 2001 (ICPSR 4043) and November 2001 (ICPSR 4044). These three supplements comprise the 2001-2002 waves of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

All household members age 15 years and older who had completed the basic CPS monthly items were eligible for the TUS, which consisted of items PES32 through PES77. The TUS was mainly designed to be a proxy response survey, meaning a single respondent could provide answers for all eligible household members. Unique to the TUS design were also a set of self-respondent questions. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for questions on the topics of smoking status (items PES32-PES34) and the use of other tobacco products; for example, pipes, cigars, chewing tobacco, and snuff (items PES62A-PES63B).

Additionally, self-respondents were asked various questions depending on their smoking status -- former, everyday, or occasional (items PES36-PES46 and PES55-PES61). Current everyday and occasional smokers were then asked whether the medical community had advised them to quit smoking or if they were planning to quit in the near future (items PES47-PES54). Self-respondents were further queried on smoking policies in their work place (items PES67-PES71), smoking rules in the home (item PES73) and questions on opinions about smoking (items PES72, PES75-PES77).

Administrative information was collected on who the proxy respondents were, the language in which the interview was conducted, and the survey method (telephone vs. personal-visit interviews; Computer Assisted Telephone Interviewing (CATI) vs. Computer Assisted Personal Interviewing (CAPI)). Demographic information collected includes age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the February 2003 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in June 2003 (ICPSR 4527) and November 2003 (ICPSR 4528). These three supplements comprise the 2003 wave of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

The TUS, like most CPS supplements, was designed to be a proxy response supplement, meaning a single respondent could provide answers for all eligible household members, provided the respondent was a household member 15 years of age or older. Unique to the TUS design were also a set of self-respondent supplement questions. All household members age 15 years and older who had completed the basic CPS core items were eligible for the February 2003 supplement items.

The TUS consisted of items PEA1 through PEK5. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for certain items. Information was collected from proxies on topics such as smoking status (items PEA1-PEA3) and the use of other tobacco-related products, such as pipes, cigars, chewing tobacco, and snuff (items PEJ1a -PEJ2a).

In addition to these smoking status and other tobacco use questions, self-respondents were queried on the following topics depending on their smoking/tobacco use status (i.e., every day, some days, or former cigarette smokers and/or users of other non-cigarette tobacco products):

• Smoking history

• Current cigarette smoking prevalence and consumption

• Type of cigarettes smoked

• Price of last pack/carton of cigarettes purchased and state where purchased

• Medical and dental advice to quit smoking

• Attempts and intentions to quit smoking cigarettes and/or other forms of tobacco use

• Workplace smoking policies and smoking rules in the home

• Attitudes toward smoking in public places

Another generally unique feature to the 2003 TUS-CPS was the administration of questions to former smokers on their previous level of addiction, products/resources/methods used to quit smoking, and advice from health professionals. This feature enables comparisons between characteristics of former smokers (or successful quitters) and current smokers attempting to quit.

Administrative information was collected on who the proxy respondents were, the language in which the interview was conducted, and the survey method (telephone vs. personal-visit interviews; Computer Assisted Telephone Interviewing (CATI) vs. Computer Assisted Personal Interviewing (CAPI)). Demographic information collected include age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the January 2007 basic CPS questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in May 2006 (ICPSR 24781) and August 2006 (ICPSR 24782). These three supplements comprise the 2006-2007 waves of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

The TUS, like most CPS supplements, was designed to be a proxy response supplement, meaning a single respondent could provide answers for all eligible household members, provided the respondent was a household member 15 years of age or older. Unique to the TUS design were also a set of self-respondent supplement questions. All household members age 18 years and older who had completed the basic CPS core items were eligible for the January 2007 supplement items. Beginning in August 2006, 15-17 year old respondents were phased out of the TUS and they were entirely omitted from the January 2007 sample due to Census Bureau budget constraints (but remained for the May and August 2006 waves).

The TUS consisted of items PEA1 through SINTTP. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for certain items. Information was collected from proxies on topics such as smoking status (items PEA1-PEA3) and the use of other tobacco-related products, such as pipes, cigars, chewing tobacco, and snuff (items PEAJ1A1-PEAJ1A4 and PEJ2A1-PEJSA4).

In addition to these smoking and other tobacco use status questions, self-respondents were queried on the following topics depending on their smoking/tobacco use status (i.e., every day, some days, or former cigarette smokers and/or users of other non-cigarette tobacco products):

• Smoking history

• Current cigarette smoking prevalence and consumption

• Type of cigarettes smoked

• Price of last pack/carton of cigarettes purchased and state of purchase

• Medical and dental advice to quit smoking

• Attempts and intentions to quit smoking cigarettes and/or other forms of tobacco use

• Awareness of 1-800-QUIT-NOW

• Workplace smoking policies and smoking rules in the home

• Attitudes toward smoking in public places

Another generally unique feature to the 2006-2007 TUS-CPS was the administration of questions to former smokers on their previous level of addiction, use of quitlines, and advice from health professionals. This feature enables comparisons between characteristics of former smokers (or successful quitters) and current smokers attempting to quit.

Demographic information collected include age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

The Current Population Survey Tobacco Use Supplement data collection from January 2015 is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a Tobacco Use Supplement (TUS) survey. The TUS 2014-2015 Wave consists of three collections: July 2014, January 2015, and May 2015.

The CPS, administered monthly, is the source of the official government statistics on employment and unemployment. From time to time, additional questions are included on health, education, and previous work experience. The Tobacco Use Supplement to the CPS is a National Cancer Institute sponsored survey of tobacco use that has been administered as part of the US Census Bureau's CPS approximately every 3-4 years since 1992-1993.

Similar to other CPS supplements, the Tobacco Use Supplement was designed for both proxy and self-respondents. All CPS household members age 18 and older who completed CPS core items in January 2015 were eligible for the supplement items. A new feature for the 2014-2015 cycle included random selection of self-interviewed respondents in larger households to reduce respondent burden. If the household had only 1 supplement eligible member then that person was selected for self-interview. If the household had only 2 supplement eligible members, then both of them were selected for self-interview. If the household had 3 or 4 supplement eligible members, then 2 of them were randomly selected for self-interview and the remaining were interviewed by proxy. If the household had more than 4 supplement eligible members, then 3 of them were randomly selected for self-interview and the rest of the eligible respondents were interviewed by proxy.

Those selected for self-interview were eligible for the entire supplement, whereas proxy respondents were only eligible for an abbreviated interview. Occasionally, those persons to be interviewed by proxy, if available for self- interview, were interviewed directly but asked the abbreviated proxy path questions.

Both proxy and self-respondents were asked about their smoking status and the use of other tobacco products. For self-respondents only, different questions were asked depending on their tobacco use status: for former/current smokers, questions were asked about type of cigarettes smoked, measures of addiction, attempts to quit smoking, methods and treatments used to quit smoking, and if they were planning to quit in the future. All self-respondents were asked about smoking policy at their work place and their attitudes towards smoking in different locations.

Demographic information within this collection includes age, sex, race, Hispanic origin, marital status, veteran status, immigration status, educational background, employment status, occupation, and income.

The Current Population Survey Tobacco Use Supplement data collection from July 2015 is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a Tobacco Use Supplement (TUS) survey. The TUS 2014-2015 Wave consists of three collections: July 2014, January 2015, and May 2015.

The CPS, administered monthly, is the source of the official government statistics on employment and unemployment. From time to time, additional questions are included on health, education, and previous work experience. The Tobacco Use Supplement to the CPS is a National Cancer Institute sponsored survey of tobacco use that has been administered as part of the US Census Bureau's CPS approximately every 3-4 years since 1992-1993.

Similar to other CPS supplements, the Tobacco Use Supplement was designed for both proxy and self-respondents. All CPS household members age 18 and older who completed CPS core items in July 2014 were eligible for the supplement items. A new feature for the 2014-2015 cycle included random selection of self-interviewed respondents in larger households to reduce respondent burden. If the household had only 1 supplement eligible member then that person was selected for self-interview. If the household had only 2 supplement eligible members, then both of them were selected for self-interview. If the household had 3 or 4 supplement eligible members, then 2 of them were randomly selected for self-interview and the remaining were interviewed by proxy. If the household had more than 4 supplement eligible members, then 3 of them were randomly selected for self-interview and the rest of the eligible respondents were interviewed by proxy.

Those selected for self-interview were eligible for the entire supplement, whereas proxy respondents were only eligible for an abbreviated interview. Occasionally, those persons to be interviewed by proxy, if available for self-interview, were interviewed directly but asked the abbreviated proxy path questions.

Both proxy and self-respondents were asked about their smoking status and the use of other tobacco products. For self-respondents only, different questions were asked depending on their tobacco use status: for former/current smokers, questions were asked about type of cigarettes smoked, measures of addiction, attempts to quit smoking, methods and treatments used to quit smoking, and if they were planning to quit in the future. All self-respondents were asked about smoking policy at their work place and their attitudes towards smoking in different locations.

Demographic information within this collection includes age, sex, race, Hispanic origin, marital status, veteran status, immigration status, educational background, employment status, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the June 2001 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in November 2001 (ICPSR 4044) and February 2002 (ICPSR 4031). These three supplements comprise the 2001-2002 waves of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

All household members age 15 years and older who had completed the basic CPS monthly items were eligible for the TUS, which consisted of items PES32 through PES77. The TUS was mainly designed to be a proxy response survey, meaning a single respondent could provide answers for all eligible household members. Unique to the TUS design were also a set of self-respondent questions. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for questions on the topics of smoking status (items PES32-PES34) and the use of other tobacco products; for example, pipes, cigars, chewing tobacco, and snuff (items PES62A-PES63B).

Additionally, self-respondents were asked various questions depending on their smoking status -- former, everyday, or occasional (items PES36-PES46 and PES55-PES61). Current everyday and occasional smokers were then asked whether the medical community had advised them to quit smoking or if they were planning to quit in the near future (items PES47-PES54). Self-respondents were further queried on smoking policies in their work place (items PES67-PES71), smoking rules in the home (item PES73) and questions on opinions about smoking (items PES72, PES75-PES77).

Administrative information was collected on who the proxy respondents were, the language in which the interview was conducted, and the survey method (telephone vs. personal-visit interviews; Computer Assisted Telephone Interviewing (CATI) vs. Computer Assisted Personal Interviewing (CAPI)). Demographic information collected includes age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the June 2003 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in February 2003 (ICPSR 4526) and November 2003 (ICPSR 4528). These three supplements comprise the 2003 wave of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

The TUS, like most CPS supplements, was designed to be a proxy response supplement, meaning a single respondent could provide answers for all eligible household members, provided the respondent was a household member 15 years of age or older. Unique to the TUS design were also a set of self-respondent supplement questions. All household members age 15 years and older who had completed the basic CPS core items were eligible for the June 2003 supplement items.

The TUS consisted of items PEA1 through PEK5. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for certain items. Information was collected from proxies on topics such as smoking status (items PEA1-PEA3) and the use of other tobacco-related products, such as pipes, cigars, chewing tobacco, and snuff (items PEJ1a -PEJ2a).

In addition to these smoking status and other tobacco use questions, self-respondents were queried on the following topics depending on their smoking/tobacco use status (i.e., every day, some days, or former cigarette smokers and/or users of other non-cigarette tobacco products):

• Smoking history

• Current cigarette smoking prevalence and consumption

• Type of cigarettes smoked

• Price of last pack/carton of cigarettes purchased and state where purchased

• Medical and dental advice to quit smoking

• Attempts and intentions to quit smoking cigarettes and/or other forms of tobacco use

• Workplace smoking policies and smoking rules in the home

• Attitudes toward smoking in public places

Another generally unique feature to the 2003 TUS-CPS was the administration of questions to former smokers on their previous level of addiction, products/resources/methods used to quit smoking, and advice from health professionals. This feature enables comparisons between characteristics of former smokers (or successful quitters) and current smokers attempting to quit.

Administrative information was collected on who the proxy respondents were, the language in which the interview was conducted, and the survey method (telephone vs. personal-visit interviews; Computer Assisted Telephone Interviewing (CATI) vs. Computer Assisted Personal Interviewing (CAPI)). Demographic information collected include age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the May 2006 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in August 2006 (ICPSR 24782) and January 2007 (ICPSR 24783). These three supplements comprise the 2006-2007 waves of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

The TUS -- like most CPS supplements -- was designed to be a proxy response supplement, meaning a single respondent could provide answers for all eligible household members, provided the respondent was a household member 15 years of age or older. Unique to the TUS design were also a set of self-respondent supplement questions. All household members age 15 years and older who had completed the basic CPS core items were eligible for the May 2006 supplement items. Beginning in August 2006, 15-17 year old respondents were phased out of the TUS and they were entirely omitted from the January 2007 sample due to Census Bureau budget constraints.

The TUS consisted of items PEA1 through SINTTP. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for certain items. Information was collected from proxies on topics such as smoking status (items PEA1-PEA3) and the use of other tobacco-related products, such as pipes, cigars, chewing tobacco, and snuff (items PEAJ1A1-PEAJ1A4 and PEJ2A1-PEJSA4).

In addition to these smoking and other tobacco use status questions, self-respondents were queried on the following topics depending on their smoking/tobacco use status (i.e., every day, some days, or former cigarette smokers and/or users of other non-cigarette tobacco products):

• Smoking history

• Current cigarette smoking prevalence and consumption

• Type of cigarettes smoked

• Price of last pack/carton of cigarettes purchased and state of purchase

• Medical and dental advice to quit smoking

• Attempts and intentions to quit smoking cigarettes and/or other forms of tobacco use

• Awareness of 1-800-QUIT-NOW

• Workplace smoking policies and smoking rules in the home

• Attitudes toward smoking in public places

Another generally unique feature to the 2006-2007 TUS-CPS was the administration of questions to former smokers on their previous level of addiction, use of quitlines, and advice from health professionals. This feature enables comparisons between characteristics of former smokers (or successful quitters) and current smokers attempting to quit.

Demographic information collected include age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

The Current Population Survey Tobacco Use Supplement data collection from May 2015 is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a Tobacco Use Supplement (TUS) survey. The TUS 2014-2015 Wave consists of three collections: July 2014, January 2015, and May 2015.

The CPS, administered monthly, is the source of the official government statistics on employment and unemployment. From time to time, additional questions are included on health, education, and previous work experience. The Tobacco Use Supplement to the CPS is a National Cancer Institute sponsored survey of tobacco use that has been administered as part of the US Census Bureau's CPS approximately every 3-4 years since 1992-1993.

Similar to other CPS supplements, the Tobacco Use Supplement was designed for both proxy and self-respondents. All CPS household members age 18 and older who had completed CPS core items were eligible for the supplement items. A new feature for the 2014-2015 cycle included random selection of self-interviewed respondents in larger households to reduce respondent burden. If the household had only 1 supplement eligible member then that person was selected for self-interview. If the household had only 2 supplement eligible members, then both of them were selected for self-interview. If the household had 3 or 4 supplement eligible members, then 2 of them were randomly selected for self-interview and the remaining were interviewed by proxy. If the household had more than 4 supplement eligible members, then 3 of them were randomly selected for self-interview and the rest of the eligible respondents were interviewed by proxy.

Those selected for self-interview were eligible for the entire supplement, whereas proxy respondents were only eligible for an abbreviated interview. Occasionally, those persons to be interviewed by proxy, if available for self- interview, were interviewed directly but asked the abbreviated proxy path questions.

Both proxy and self-respondents were asked about their smoking status and the use of other tobacco products. For self-respondents only, different questions were asked depending on their tobacco use status: for former/current smokers, questions were asked about type of cigarettes smoked, measures of addiction, attempts to quit smoking, methods and treatments used to quit smoking, and if they were planning to quit in the future. All self-respondents were asked about smoking policy at their work place and their attitudes towards smoking in different locations.

Demographic information within this collection includes age, sex, race, Hispanic origin, marital status, veteran status, immigration status, educational background, employment status, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the November 2001 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in June 2001 (ICPSR 4043) and February 2002 (ICPSR 4031). These three supplements comprise the 2001-2002 waves of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

All household members age 15 years and older who had completed the basic CPS monthly items were eligible for the TUS, which consisted of items PES32 through PES77. The TUS was mainly designed to be a proxy response survey, meaning a single respondent could provide answers for all eligible household members. Unique to the TUS design were also a set of self-respondent questions. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for questions on the topics of smoking status (items PES32-PES34) and the use of other tobacco products; for example, pipes, cigars, chewing tobacco, and snuff (items PES62A-PES63B).

Additionally, self-respondents were asked various questions depending on their smoking status -- former, everyday, or occasional (items PES36-PES46 and PES55-PES61). Current everyday and occasional smokers were then asked whether the medical community had advised them to quit smoking or if they were planning to quit in the near future (items PES47-PES54). Self-respondents were further queried on smoking policies in their work place (items PES67-PES71), smoking rules in the home (item PES73) and questions on opinions about smoking (items PES72, PES75-PES77).

Administrative information was collected on who the proxy respondents were, the language in which the interview was conducted, and the survey method (telephone vs. personal-visit interviews; Computer Assisted Telephone Interviewing (CATI) vs. Computer Assisted Personal Interviewing (CAPI)). Demographic information collected includes age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

This data collection is comprised of responses from two sets of survey questionnaires, the basic Current Population Survey (CPS) and a survey administered as a supplement to the November 2003 questionnaire on the topic of tobacco use in the United States. The Tobacco Use Supplement (TUS), sponsored by the National Cancer Institute and the Centers for Disease Control and Prevention, was also administered in February 2003 (ICPSR 4526) and June 2003 (ICPSR 4527). These three supplements comprise the 2003 wave of TUS data.

The basic CPS, administered monthly, collects labor force data about the civilian noninstitutional population living in the United States. Moreover, the CPS provides current estimates of the economic status and activities of this population which includes estimates of total employment (both farm and nonfarm), nonfarm self-employed persons, domestics, and unpaid helpers in nonfarm family enterprises, wage and salaried employees, and estimates of total unemployment. Data from the CPS are provided for the week prior to the administration of the survey.

The TUS, like most CPS supplements, was designed to be a proxy response supplement, meaning a single respondent could provide answers for all eligible household members, provided the respondent was a household member 15 years of age or older. Unique to the TUS design were also a set of self-respondent supplement questions. All household members age 15 years and older who had completed the basic CPS core items were eligible for the November 2003 supplement items.

The TUS consisted of items PEA1 through PEK5. Self-respondents were eligible for the entire supplement, whereas proxy respondents were only eligible for certain items. Information was collected from proxies on topics such as smoking status (items PEA1-PEA3) and the use of other tobacco-related products, such as pipes, cigars, chewing tobacco, and snuff (items PEJ1a-PEJ2a).

In addition to these smoking status and other tobacco use questions, self-respondents were queried on the following topics depending on their smoking/tobacco use status (i.e., every day, some days, or former cigarette smokers and/or users of other non-cigarette tobacco products):

• Smoking history

• Current cigarette smoking prevalence and consumption

• Type of cigarettes smoked

• Price of last pack/carton of cigarettes purchased and state where purchased

• Medical and dental advice to quit smoking

• Attempts and intentions to quit smoking cigarettes and/or other forms of tobacco use

• Workplace smoking policies and smoking rules in the home

• Attitudes toward smoking in public places

Another generally unique feature to the 2003 TUS-CPS was the administration of questions to former smokers on their previous level of addiction, products/resources/methods used to quit smoking, and advice from health professionals. This feature enables comparisons between characteristics of former smokers (or successful quitters) and current smokers attempting to quit.

Administrative information was collected on who the proxy respondents were, the language in which the interview was conducted, and the survey method (telephone vs. personal-visit interviews; Computer Assisted Telephone Interviewing (CATI) vs. Computer Assisted Personal Interviewing (CAPI)). Demographic information collected include age, sex, race, Hispanic origin, marital status, veteran status, educational attainment, family relationship, occupation, and income.

The Future of Families and Child Wellbeing Study (FFCWS, formerly known as the Fragile Families and Child Wellbeing Study) follows a cohort of nearly 5,000 children born in large, U.S. cities between 1998 and 2000. The study oversampled births to unmarried couples; and, when weighted, the data are representative of births in large U.S. cities at the turn of the century. The FFCWS was originally designed to address four questions of great interest to researchers and policy makers:

1. What are the conditions and capabilities of unmarried parents, especially fathers?
2. What is the nature of the relationships between unmarried parents?
3. How do children born into these families fare?
4. How do policies and environmental conditions affect families and children?

The FFCWS consists of interviews with mothers, fathers, and/or primary caregivers at birth and again when children are ages 1, 3, 5, 9, 15, and 22. The parent interviews collected information on attitudes, relationships, parenting behavior, demographic characteristics, health (mental and physical), economic and employment status, neighborhood characteristics, and program participation. Beginning at age 9, children were interviewed directly (either during the home visit or on the telephone). The direct child interviews collected data on family relationships, home routines, schools, peers, and physical and mental health, as well as health behaviors.

A collaborative study of the FFCWS, the In-Home Longitudinal Study of Pre-School Aged Children (In-Home Study) collected data from a subset of the FFCWS Core respondents at the Year 3 and 5 follow-ups to ask how parental resources in the form of parental presence or absence, time, and money influence children under the age of 5. The In-Home Study collected information on a variety of domains of the child's environment, including: the physical environment (quality of housing, nutrition and food security, health care, adequacy of clothing and supervision) and parenting (parental discipline, parental attachment, and cognitive stimulation). In addition, the In-Home Study also collected information on several important child outcomes, including anthropometrics, child behaviors, and cognitive ability. This information was collected through interviews with the child's primary caregiver, and direct observation of the child's home environment and the child's interactions with his or her caregiver.

Similar activities were conducted during the Year 9 follow-up. At the Year 15 follow-up, a condensed set of home visit activities were conducted with a subsample of approximately 1,000 teens. Teens who participated in the In-Home Study were also invited to participate in a Sleep Study and were asked to wear an accelerometer on their non-dominant wrist for seven consecutive days to track their sleep (Sleep Actigraphy Data) and that day's behaviors and mood (Daily Sleep Actigraphy and Diary Survey Data).

An additional collaborative study collected data from the child care provider (Year 3) and teacher (Years 9 and 15) through mail-based surveys. Saliva samples were collected at Year 9 and 15 (Biomarker file and Polygenic Scores). The Study of Adolescent Neural Development (SAND) COVID Study began data collection in May 2020 following the onset of the COVID-19 pandemic. It included online surveys with the young adult and their primary caregiver.

The FFCWS began its seventh wave of data collection in October 2020, around the focal child's 22nd birthday. Data collection and interviews continued through January 2024. The Year 22 wave included a young adult (YA) survey with the original focal child and a primary caregiver (PCG) survey. Data were also collected on the children of the original focal child (referred to as Generation 3, or G3).

In 2017, the FFCWS team announced the Fragile Families (FF) Challenge, a collaborative effort in which participants were tasked with using machine learning methods and FFCWS data (Baseline to Year 9) to build a model that would predict six key outcomes at Year 15. Materials used in the FF Challenge have been archived in this collection.

Documentation for these files is available on the FFCWS website under Data and Documentation. For details of updates made to the FFCWS data files, please see the project's Data Alerts page.

Data collection for the Future of Families and Child Wellbeing Study was supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) of the National Institutes of Health under award numbers R01HD36916, R01HD39135, and R01HD40421, as well as a consortium of private foundations.

Below is the citation for use of the FFCWS data accessed through ICPSR. For information on additional citation requirements when using FFCWS in publications, please refer to this FAQ on the FFCWS project site.

The Health and Aging in Africa: A Longitudinal Study of an INDEPTH Community in South Africa (HAALSI) study is a population-based survey that aims to examine and characterize a population of older men and women in rural South Africa with respect to health, physical and cognitive function, aging, and well-being, in harmonization with other Health and Retirement Studies.

The baseline survey was conducted among 5,059 men and women aged 40 years or older, who were sampled from within the existing framework of the Agincourt health and socio-demographic surveillance system (AHDSS), in rural Mpumalanga province, South Africa. Survey data were collected on cognitive and physical functioning, social networks, cardiometabolic disease and risk factors, HIV and HIV risk, and economic well-being. The survey also included anthropometric measures and point-of-care blood tests for hemoglobin, glucose and lipids. Dried bloodspots (DBS) were collected at the survey and later tested for HIV, HIV viral load, glucose and CRP. A sub-sample had more extensive laboratory follow-up testing, which will be available in future data releases. A second wave of the survey was administered in 2018 through 2019, and a third wave of the survey was administered in 2021 through 2022.

Demographic information includes age, sex, income, education, marital status, number of children, and employment.

Harvard dataverse hosts an additional restricted-use dataset which compliments this collection, the HAALSI Baseline HIV Biomarker Data; users interested in obtaining these data must request access based on the terms outlined in the data use agreement.

These data are part of NACJD's Fast Track Release and are distributed as they were received from the data depositor. The files have been zipped by NACJD for release, but not checked or processed except for the removal of direct identifiers. Users should refer to the accompanying readme file for a brief description of the files available with this collection and consult the investigators if further information is needed.

This study is a secondary analysis (syntax only, no data) of Research on Pathways to Desistance [Maricopa County, AZ and Philadelphia County, PA]: Subject Measures, 2000-2010 (ICPSR 29961) and Research on Pathways to Desistance [Maricopa County, AZ and Philadelphia County, PA]: Calendar Data, 2000-2010 [Restricted] (ICPSR 32282).

The purpose of this study was to further existing knowledge of juvenile justice intervention and how juvenile justice intervention is related to positive outcomes during the transition to adulthood. This study examines three main aims using data from the Pathways to Desistance study, which followed a sample of serious adolescent offenders for seven years to examine the desistance process. First, trajectories of secure institutional placement for serious offenders during the study period were identified. Second, trajectories of gainful activities for serious adolescent offenders during the study period were identified. Gainful activities were defined as working or attending school. Third, factors associated with turning points in the gainful activities trajectories were explored. In the course of estimating the gainful activities trajectories, there appeared to be a key moment, around year 3, where multiple trajectories with moderate levels of engagement in gainful activities diverged. Together, these three aims will inform how juvenile justice intervention is related to positive outcomes during the transition to adulthood and identify factors that may be related to positive outcomes and critical turning points in the trajectories of serious adolescent offenders.

Group differences were examined by testing bivariate differences in a broad range of variables: demographic variables (gender, age, and race/ethnicity); study site and year of interview; characteristics of prior service receipt at baseline (location and orientation); school, family and neighborhood characteristics; characteristics of the offense and offense history; individual factors (mental health and substance use symptoms); and risk scores.

In 1995-1996, the MacArthur Midlife Research Network carried out a national survey of 7,108 Americans aged 25 to 74 (MIDLIFE IN THE UNITED STATES (MIDUS), 1995-1996 [ICPSR 2760]). The purpose of the study was to investigate the role of behavioral, psychological, and social factors in understanding age-related differences in physical and mental health. The study was innovative for its broad scientific scope, its diverse samples (which included twins and the siblings of main sample respondents), and its creative use of in-depth assessments in key areas (e.g., daily stress and cognitive functioning). A description of the study and findings from it are available at http://www.midus.wisc.edu. With support from the National Institute on Aging, a longitudinal follow-up of the original MIDUS samples: core sample (N = 3,487), metropolitan over-samples (N = 757), twins (N = 925 complete pairs), and siblings (N = 950), was conducted in 2004-2006. Guiding hypotheses for it, at the most general level, were that behavioral and psychosocial factors are consequential for physical and mental health. MIDUS 2 respondents were aged 35 to 86. Data collection largely repeated baseline assessments (e.g., phone interview and extensive self-administered questionnaire), with additional questions in selected areas (e.g., cognitive functioning, optimism and coping, stressful life events, and caregiving). To add refinements to MIDUS 2, an African American sample (N = 592) was recruited from Milwaukee, Wisconsin, who participated in a personal interview and completed a questionnaire paralleling the above assessments. Survey data for the Milwaukee sample are available in a separate project [ICPSR 22840]. Also administered was a modified form of the mail questionnaire, via telephone, to respondents who did not complete a self-administered questionnaire.

In 2011-2014, the MIDUS Refresher study recruited a national probability sample of 3,577 adults, aged 25 to 74, designed to replenish the original MIDUS 1 baseline cohort and paralleling the five decadal age groups of the MIDUS 1 baseline survey [ICPSR 2760]. The MIDUS Refresher survey employed the same comprehensive assessments as those assembled on the existing MIDUS sample, but with additional questions about the effect of the economic recession of 2008-09.

The MIDUS Refresher collection is split into two datasets: Aggregate Data and Coded Text Data. The Coded Text Dataset provides coded responses to open-ended question items in the Aggregate Dataset. The survey data collection (Project 1) [MIDUS, ICPSR 2760] consisted of a 30-minute phone interview followed by two 50-page mailed self-administered questionnaires. Survey data were collected on demographic, psycho-social, and physical and mental health information. This new crosssectional MIDUS sample allows the examination of period effects on health (mental and physical) related to the economic recession by comparing the pre-recession MIDUS 1 sample with the post-recession MIDUS Refresher sample. A further objective of the MIDUS Refresher sample was to strengthen cross-project analyses in MIDUS by increasing the sample sizes available for testing hypotheses dealing with the interplay of key factors (e.g., socioeconomic status, gender, psychosocial factors, biological factors) in mid- and laterlife health. To that end, the MIDUS Refresher sample followed the same multi-disciplinary protocol established in the main MIDUS sample, in that after completing the survey protocol respondents were asked to complete a cognitive assessment by phone (Project 3) [MIDUS 3, ICPSR 36346] and later became eligible to participate in daily diary assessments (Project 2) [MIDUS 2, ICPSR 4652] biomarker assessments (Project 4) [MIDUS 2: Biomarker Project, ICPSR 29282] and neuroscience assessments (Project 5) [MIDUS 2: Neuroscience Project, ICPSR 28683].

The MIDUS Refresher was funded by the National Institute on Aging as two separate but related efforts: The MIDUS Refresher younger decades (MRY), was fielded in November, 2011, and recruited over 2,100 new participants aged 25 to 54; Funding was later added for the MIDUS Refresher older decades (MRO), which was fielded in June, 2013 and recruited over 1,400 new participants aged 55 to 74.

Demographic variables include age, sex, gender, race, religion, and marital status.

The MIDUS Refresher study Survey (2011-2014 ICPSR 36532) recruited a national probability sample of 3,577 adults, aged 25 to 74, designed to replenish the original MIDUS 1 baseline cohort and paralleling the five decadal age groups of the MIDUS 1 baseline survey (ICPSR 2760). The MIDUS Refresher survey employed the same comprehensive assessments as those assembled on the core longitudinal MIDUS sample, but with additional questions about impacts of the economic recession of 2008-09. The MIDUS Refresher Biomarker study (2012-2016) obtained data from 863 respondents (n=746 Main sample, n=117 African Americans from Milwaukee) who completed the MIDUS Refresher Survey.

The purpose of the Refresher Biomarker Project (Project 4) parallels that of the MIDUS 2 Biomarker project (ICPSR 29282), which collected comprehensive biological assessments on a subsample of MIDUS respondents, thus facilitating analyses that integrate behavioral and psychosocial factors with biological regulation/dysregulation, broadly defined. The aim was to use such data to explicate biopsychosocial pathways that contributed to diverse health outcomes. A further theme was to examine period effects on health (mental and physical) related to the economic recession by comparing the pre-recession MIDUS sample with the post-recession MIDUS Refresher sample. A further objective of the MIDUS Refresher sample was to strengthen cross-project analyses by increasing the sample sizes available for testing hypotheses regarding the interplay of key factors (e.g., socioeconomic status, gender, psychosocial factors, biological factors) in mid- and later-life health.

Biomarker data collection was carried out at hypothalamic-pituitary-adrenal axis, the autonomic nervous system, the immune system, cardiovascular system, musculoskeletal system, antioxidants, and three General Clinical Research Centers (at UCLA, University of Wisconsin, and Georgetown University). The biomarkers reflect functioning of the metabolic processes. Our specimens (fasting blood draw, 12-hour urine, saliva) allowed for assessment of multiple indicators within these major systems. The protocol also included assessments by clinicians or trained staff, including vital signs, morphology, functional capacities including 3 dimensional gait analysis, bone densitometry, body composition, ankle brachial index, medication usage, and a physical exam. Project staff obtained indicators of heart-rate variability, beat to beat blood pressure, respiration, and salivary cortisol assessments during an experimental protocol that included both a cognitive and orthostatic challenge. Finally, to augment the self-reported data collected in Survey (Project 1), participants completed a medical history, self-administered questionnaire, and self-reported sleep assessments. For respondents at one site (UW-Madison), objective sleep assessments were also obtained with an Actiwatch(R) activity monitor.

The National Institute on Drug Abuse (NIDA) funded RADAR in 2014 to collect multilevel, longitudinal data and biospecimens from an ethnically and racially diverse cohort of young, sexual and gender minorities (SGM; e.g., men who have sex with men (MSM), transgender women, gender non-conforming individuals) who were assigned male at birth (AMAB) (current core cohort n=1,113). The primary objective of this study is to apply a multilevel perspective to a syndemic of health issues associated with human immunodeficiency virus (HIV) in this population. The multilevel design focuses on individual, dyadic (i.e., sexual and romantic relationships), network (i.e., social, drug, and sexual connections) and biologic factors that may be associated with HIV. The cohort contains both HIV-negative and HIV-positive individuals, which allows for the development of a repository of biospecimens and HIV sequence data from both pre-infection and post-infection visits that will help facilitate future projects evaluating substance use, HIV risk, and pathogenesis.

A multiple cohort, accelerated longitudinal design was utilized by initially enrolling two existing SGM cohorts and then expanded through the use of convenience and snowball sampling methods. Enrollment criteria varied slightly based on the recruitment method, but overall inclusion criteria required participants to be AMAB, between 16 and 29 years of age, report having had sex with a man in the prior year or identify as a SGM, live in the Chicago metropolitan area, and be an English speaker. Study recruitment opened in February 2015. Participants are followed through the developmental period of late adolescence to early adulthood, which is a critical period of initiation and acceleration of sexual behavior and substance use. Study visits occur every six months.

The Multi-Site Adult Drug Court Evaluation (MADCE) study included 23 drug courts and 6 comparison sites selected from 8 states across the country. The purpose of the study was to: (1) Test whether drug courts reduce drug use, crime, and multiple other problems associated with drug abuse, in comparision with similar offenders not exposed to drug courts, (2) address how drug courts work and for whom by isolating key individual and program factors that make drug courts more or less effective in achieving their desired outcomes, (3) explain how offender attitudes and behaviors change when they are exposed to drug courts and how these changes help explain the effectiveness of drug court programs, and (4) examine whether drug courts generate cost savings.

Offenders in all 29 sites were surveyed in 3 waves, at baseline, 6 months later, and 18 months after enrollment. The research comprises three major components: process evaluation, impact evaluation, and a cost-benefit analysis. The process evaluation describes how the 23 drug court sites vary in program eligibility, supervision, treatment, team collaboration, and other key policies and practices. The impact evaluation examines whether drug courts produce better outcomes than comparison sites and tests which court policies and offender attitudes might explain those effects. The cost-benefit analysis evaluates drug court costs and benefits.

This collection contains data from the Multi-site Family Study on Incarceration, Parenting and Partnering [MSF-IP]. The MSF-IP is an evaluation of a grant program funded by the Office of Family Assistance (OFA) within the U.S. Department of Health and Human Services (HHS), Administration for Children and Families (ACF) to promote or sustain healthy relationships and to strengthen families in which a father was incarcerated or otherwise involved with the criminal justice system (e.g., recently released or on parole or probation). From 2006-2011, grantees were required to serve justice-involved fathers and their committed partners with services to promote healthy marriage; they were also permitted to provide activities to support parenting and foster economic stability.

The MFS-IP evaluation was funded to document program implementation and the impact of programming on outcomes such as relationship quality and stability, parenting and co-parenting, family financial well-being, and recidivism. This collection includes data from the impact study, conducted across five grantees: the Indiana Department of Correction, the RIDGE Project (Ohio), the New Jersey Department of Corrections, the Osborne Association (New York), and the Minnesota Council on Crime and Justice. The collection includes de-identified interview data for 1,991 men and 1,482 intimate and co-parenting partners.

The interviews took place from December 2008 through August 2014. Couples were first interviewed during the male partner's incarceration (with the timing of baseline interviews not related to the man's admission or release date in most sites) and then interviewed again nine and 18 months after baseline. In the two largest sites (Indiana and Ohio), an additional 34-month follow-up interview was conducted. The interviews were similar in content at each interview wave and for the male and female interviews, but differed based on male partner's trajectory of incarceration and release over the follow-up period.

Topics within this collection include demographics, personal characteristics and attitudes, criminal history and behavior, incarceration experiences (including family contact during incarceration), program and service receipt, expectations for release, family structure and functioning, intimate relationship quality, parenting and co-parenting quality, child well-being, employment, housing, substance use, and experiences with reentry.

The National Comorbidity Survey Replication Adolescent Supplement (NCS-A) was designed to estimate the lifetime-to-date and current prevalence, age-of-onset distributions, course, and comorbidity of DSM-IV disorders in the child and adolescent years of life among adolescents in the United States; to identify risk and protective factors for the onset and persistence of these disorders; to describe patterns and correlates of service use for these disorders; and to lay the groundwork for subsequent follow-up studies that can be used to identify early expressions of adult mental disorders.

The core NCS-A interview schedule was an adaptation of the World Health Organization Composite International Diagnostic Interview (CIDI). NCS-A also administered the non-verbal subtest (Matrices subtest) of the Kaufman Brief Intelligence Test (K-BIT).

In addition to interviewing adolescents, information was collected from a parent or a parent surrogate to obtain an additional perspective on the adolescent's mental health and its correlates. Information from parents focused on the five adolescent disorders for which previous methodological research has most consistently shown that parental reports are important for making diagnoses: attention-deficit/hyperactivity disorder, conduct disorder, oppositional defiant disorder, major depressive episode, and dysthymic disorder.

Demographic information collected by NCS-A includes age, citizenship status, country of birth, criminal history, ethnicity, grandparents' country of birth, language(s) spoken in the home, parents' country of birth, race, religion, and sex.

The data collection contains six data files: (1) data for the adolescent household and school respondents; (2) data for the parents who responded to the long self-administered questionnaire; (3) data for the parents who responded to both the long self-administered questionnaire and short telephone interview; (4) diagnostic variables derived from the data collected from the adolescents and parents; (5) K-BIT scores normed to the NCS-A adolescent sample; and (6) raw K-BIT data.

The NCS-2 was a re-interview of 5,001 individuals who participated in the Baseline (NCS-1). The study was conducted a decade after the initial baseline survey. The aim was to collect information about changes in mental disorders, substance use disorders, and the predictors and consequences of these changes over the ten years between the two surveys. The collection contains three major sections: the main survey, demographic data, and diagnostic data.

In the main survey, respondents were asked about general physical and mental health. Questions focused on a variety of health issues, including limitations caused by respondents' health issues, substance use, childhood health, life-threatening illnesses, chronic conditions, medications taken in the past 12 months, level of functioning and symptoms experienced in the past 30 days, and any services used by the respondents since the (NCS-1). Additional questions focused on mental disorders including depression, bipolar disorder, specific and social phobias, generalized anxiety, intermittent explosive disorder, suicidality, post-traumatic stress disorder, neurasthenia, pre-menstrual dysphoric disorder, attention deficit/hyperactivity disorder, oppositional defiant disorder, conduct disorder, and separation anxiety. Respondents were also asked about their lives in general, with topics including employment, finances, marriage, children, their social lives, and stressful life events experienced in the past 12 months. Additionally, two personality assessments were included consisting of respondents' opinions on whether various true/false statements accurately described their personalities. Another focus of the main survey dealt with substance use and abuse, nonmedical use of prescription drugs, and polysubstance use. Interview questions in the NCS-2 Main Survey were customized to each respondent based on previous responses in the Baseline (NCS-1).

The middle section contains demographic and other background information including age, education, employment, household composition, household income, marital status, and region.

The last section of the collection focused on whether respondents met diagnostic criteria for psychological disorders asked about in the main survey.

The NCS-2 was a re-interview of 5,001 individuals who participated in the Baseline (NCS-1). The study was conducted a decade after the initial baseline survey. The aim was to collect information about changes in mental disorders, substance use disorders, and the predictors and consequences of these changes over the ten years between the two surveys. The collection contains four major sections: the main survey, demographic data, diagnostic data, and state, county, and tract FIPS data.

In the main survey, respondents were asked about general physical and mental health. Questions focused on a variety of health issues, including limitations caused by respondents' health issues, substance use, childhood health, life-threatening illnesses, chronic conditions, medications taken in the past 12 months, level of functioning and symptoms experienced in the past 30 days, and any services used by the respondents since the (NCS-1). Additional questions focused on mental disorders including depression, bipolar disorder, specific and social phobias, generalized anxiety, intermittent explosive disorder, suicidality, post-traumatic stress disorder, neurasthenia, pre-menstrual dysphoric disorder, attention deficit/hyperactivity disorder, oppositional defiant disorder, conduct disorder, and separation anxiety. Respondents were also asked about their lives in general, with topics including employment, finances, marriage, children, their social lives, and stressful life events experienced in the past 12 months. Additionally, two personality assessments were included consisting of respondents' opinions on whether various true/false statements accurately described their personalities. Another focus of the main survey dealt with substance use and abuse, nonmedical use of prescription drugs, and polysubstance use. Interview questions in the NCS-2 Main Survey were customized to each respondent based on previous responses in the Baseline (NCS-1).

The second part contains demographic and other background information including age, education, employment, household composition, household income, marital status, and region.

The third part focuses on whether respondents met diagnostic criteria for psychological disorders asked about in the main survey.

The fourth part contains respondents' state, county, and tract FIPS data.

In October 2019, NACJD released a revised set of 2016 NCVS Public-Use Files. The National Crime Victimization Survey, [United States], 2016: Revised Version (ICPSR 37296) data collection contains the official 2016 NCVS data and replaces the previously published National Crime Victimization Survey, 2016 (ICPSR 36828) Public-Use Files. The initial files remain available for research purposes.

The National Crime Victimization Survey (NCVS) Series, previously called the National Crime Surveys (NCS), has been collecting data on personal and household victimization through an ongoing survey of a nationally-representative sample of residential addresses since 1973. The NCVS was designed with four primary objectives: (1) to develop detailed information about the victims and consequences of crime, (2) to estimate the number and types of crimes not reported to the police, (3) to provide uniform measures of selected types of crimes, and (4) to permit comparisons over time and types of areas. The survey categorizes crimes as "personal" or "property." Personal crimes include rape and sexual attack, robbery, aggravated and simple assault, and purse-snatching/pocket-picking, while property crimes include burglary, theft, motor vehicle theft, and vandalism. Each respondent is asked a series of screen questions designed to determine whether she or he was victimized during the six-month period preceding the first day of the month of the interview. A "household respondent" is also asked to report on crimes against the household as a whole (e.g., burglary, motor vehicle theft). The data include type of crime, month, time, and location of the crime, relationship between victim and offender, characteristics of the offender, self-protective actions taken by the victim during the incident and results of those actions, consequences of the victimization, type of property lost, whether the crime was reported to police and reasons for reporting or not reporting, and offender use of weapons, drugs, and alcohol. Basic demographic information such as age, race, gender, and income is also collected, to enable analysis of crime by various subpopulations. This version of the NCVS, referred to as the collection year, contains records from interviews conducted in the 12 months of the given year.

The National Crime Victimization Survey (NCVS) Series, previously called the National Crime Surveys (NCS), has been collecting data on personal and household victimization through an ongoing survey of a nationally-representative sample of residential addresses since 1973. The NCVS was designed with four primary objectives: (1) to develop detailed information about the victims and consequences of crime, (2) to estimate the number and types of crimes not reported to the police, (3) to provide uniform measures of selected types of crimes, and (4) to permit comparisons over time and types of areas. The survey categorizes crimes as "personal" or "property." Personal crimes include rape and sexual attack, robbery, aggravated and simple assault, and purse-snatching/pocket-picking, while property crimes include burglary, theft, motor vehicle theft, and vandalism. Each respondent is asked a series of screen questions designed to determine whether she or he was victimized during the six-month period preceding the first day of the month of the interview. A "household respondent" is also asked to report on crimes against the household as a whole (e.g., burglary, motor vehicle theft). The data include type of crime, month, time, and location of the crime, relationship between victim and offender, characteristics of the offender, self-protective actions taken by the victim during the incident and results of those actions, consequences of the victimization, type of property lost, whether the crime was reported to police and reasons for reporting or not reporting, and offender use of weapons, drugs, and alcohol. Basic demographic information such as age, race, gender, and income is also collected, to enable analysis of crime by various subpopulations. This version of the NCVS, referred to as the collection year, contains records from interviews conducted in the 12 months of the given year.

This dataset represents the revised version of the NCVS on a collection year basis for 2016. A collection year contains records from interviews conducted in the 12 months of the given year. Under the collection year format, victimizations are counted in the year the interview is conducted, regardless of the year when the crime incident occurred.

The 2016 National Crime Victimization Survey (NCVS) violent and property crime estimates were significantly higher than 2015, but it was not possible to determine the degree to which the change in rates resulted from the sample redesign rather than real changes in U.S. victimization levels. Therefore, the Bureau of Justice Statistics (BJS) examined the 2015 and 2016 victimization rates separately for new and continuing sample counties in the 2016 Criminal Victimization bulletin.

The BJS requested that the Census Bureau create a 2016 revised file with outgoing county interviews from July-December 2015, continuing county interviews from January-June 2016, and all interviews (continuing and new counties) from July-December 2016. In other words, the outgoing 2015 cases replaced the new 2016 cases in the first half of 2016. The files in this study serve as a separate research file to allow data users to make comparisons between 2015, 2016, and 2017 NCVS estimates using a nationally representative sample. It provides a sample that still represents the entire country but does not have the inflated crime rates seen in the new counties in 2016.

Downloads of Add Health require submission of the following information, which is shared with the original producer of Add Health: supervisor name, supervisor email, and reason for download. A Data Guide for this study is available as a web page and for download.

The National Longitudinal Study of Adolescent to Adult Health (Add Health), 1994-2018 [Public Use] is a longitudinal study of a nationally representative sample of U.S. adolescents in grades 7 through 12 during the 1994-1995 school year. The Add Health cohort was followed into young adulthood with four in-home interviews, the most recent conducted in 2008 when the sample was aged 24-32. Add Health combines longitudinal survey data on respondents' social, economic, psychological, and physical well-being with contextual data on the family, neighborhood, community, school, friendships, peer groups, and romantic relationships.

Add Health Wave I data collection took place between September 1994 and December 1995, and included both an in-school questionnaire and in-home interview. The in-school questionnaire was administered to more than 90,000 students in grades 7 through 12, and gathered information on social and demographic characteristics of adolescent respondents, education and occupation of parents, household structure, expectations for the future, self-esteem, health status, risk behaviors, friendships, and school-year extracurricular activities. All students listed on a sample school's roster were eligible for selection into the core in-home interview sample. In-home interviews included topics such as health status, health-facility utilization, nutrition, peer networks, decision-making processes, family composition and dynamics, educational aspirations and expectations, employment experience, romantic and sexual partnerships, substance use, and criminal activities. A parent, preferably the resident mother, of each adolescent respondent interviewed in Wave I was also asked to complete an interviewer-assisted questionnaire covering topics such as inheritable health conditions, marriages and marriage-like relationships, neighborhood characteristics, involvement in volunteer, civic, and school activities, health-affecting behaviors, education and employment, household income and economic assistance, parent-adolescent communication and interaction, parent's familiarity with the adolescent's friends and friends' parents.

Add Health data collection recommenced for Wave II from April to August 1996, and included almost 15,000 follow-up in-home interviews with adolescents from Wave I. Interview questions were generally similar to Wave I, but also included questions about sun exposure and more detailed nutrition questions. Respondents were asked to report their height and weight during the course of the interview, and were also weighed and measured by the interviewer.

From August 2001 to April 2002, Wave III data were collected through in-home interviews with 15,170 Wave I respondents (now 18 to 26 years old), as well as interviews with their partners. Respondents were administered survey questions designed to obtain information about family, relationships, sexual experiences, childbearing, and educational histories, labor force involvement, civic participation, religion and spirituality, mental health, health insurance, illness, delinquency and violence, gambling, substance abuse, and involvement with the criminal justice system. High School Transcript Release Forms were also collected at Wave III, and these data comprise the Education Data component of the Add Health study.

Wave IV in-home interviews were conducted in 2008 and 2009 when the original Wave I respondents were 24 to 32 years old. Longitudinal survey data were collected on the social, economic, psychological, and health circumstances of respondents, as well as longitudinal geographic data. Survey questions were expanded on educational transitions, economic status and financial resources and strains, sleep patterns and sleep quality, eating habits and nutrition, illnesses and medications, physical activities, emotional content and quality of current or most recent romantic/cohabiting/marriage relationships, and maltreatment during childhood by caregivers. Dates and circumstances of key life events occurring in young adulthood were also recorded, including a complete marriage and cohabitation history, full pregnancy and fertility histories from both men and women, an educational history of dates of degrees and school attendance, contact with the criminal justice system, military service, and various employment events, including the date of first and current jobs, with respective information on occupation, industry, wages, hours, and benefits. Finally, physical measurements and biospecimens were also collected at Wave IV, and included anthropometric measures of weight, height and waist circumference, cardiovascular measures such as systolic blood pressure, diastolic blood pressure, and pulse, metabolic measures from dried blood spots assayed for lipids, glucose, and glycosylated hemoglobin (HbA1c), measures of inflammation and immune function, including High sensitivity C-reactive protein (hsCRP) and Epstein-Barr virus (EBV).

Wave V data collection took place from 2016 to 2018, when the original Wave I respondents were 33 to 43 years old. For the first time, a mixed mode survey design was used. In addition, several experiments were embedded in early phases of the data collection to test response to various treatments. A similar range of data was collected on social, environmental, economic, behavioral, and health circumstances of respondents, with the addition of retrospective child health and socio-economic status questions. Physical measurements and biospecimens were again collected at Wave V, and included most of the same measures as at Wave IV.

The overall goal of Wave VI was to better understand life course trajectories, determinants, and consequences of critical dimensions of aging, health, and health disparities among U.S. early midlife adults. Data collection took place from 2022 to 2025, with participants between the ages of 39 and 51, with an average age of 44. Beyond longitudinal survey measures, newly added questions included those on cumulative stress, discrimination, despair, work-life balance, memory, physical limitations, and caregiving. Continuing from previous waves, home exams collected physical measurements and biospecimens with most of the same measures as Wave V.

The National Social Life, Health and Aging Project (NSHAP) is the first population-based study of health and social factors on a national scale, aiming to understand the well-being of older, community-dwelling Americans by examining the interactions among physical health, illness, medication use, cognitive function, emotional health, sensory function, health behaviors, and social connectedness. It is designed to provide health providers, policy makers, and individuals with useful information and insights into these factors, particularly on social and intimate relationships. The National Opinion Research Center (NORC), along with Principal Investigators at the University of Chicago, conducted more than 3,000 interviews during 2005 and 2006 with a nationally representative sample of adults aged 57 to 85. Face-to-face interviews and biomeasure collection took place in respondents' homes. The following files constitute Round 1: Core Data, Marital/Cohabiting History Data, Social Networks Data, Medications Data, and Sexual Partners Data.

Included in the Core file (Datasets 1 and 2) are demographic characteristics, such as gender, age, education, race, and ethnicity. Other topics covered respondents' social networks, social and cultural activity, physical and mental health including cognition, well-being, illness, medications and alternative therapies, history of sexual and intimate partnerships and patient-physician communication, in addition to bereavement items. In addition data was collected from respondents on the following items and modules: social activity items, physical contact module, sexual interest module, get up and go assessment of physical function and a panel of biomeasures including, weight, waist circumference, height, blood pressure, smell, saliva collection, taste, and a self-administered vaginal swab for female respondents. The Core file also contains a count of the total number of drugs taken, and a variable for each observed therapeutic category, indicating whether the respondent reported taking one or more medications in that category. These variables are derived from the information in the medications file, and thus are guaranteed to be consistent with it. The Marital/Cohabiting History file (Dataset 3) contains one record for each marriage or cohabitation identified in Section 3A of the questionnaire. The Social Networks file (Datasets 4 and 5) contains one record for each person identified on the network roster. Respondents who refused to participate in the roster or who did not identify anyone are not represented in this file. The Medications file (Dataset 6) contains one record for each item listed in the medications log (including alternative medicines and nutritional products). Respondents who did not report taking any medications or who refused to participate in this module are not represented in this file. Lastly, the Sexual Partners file (Dataset 7) contains one record for each sexual partner identified in Section 3A of the questionnaire.

NACDA also maintains a Colectica portal with the NSHAP Core data across rounds 1-3, which allows users to interact with variables across rounds and create customized subsets. Registration is required.

The National Social Life, Health and Aging Project (NSHAP) is the first population-based study of health and social factors on a national scale, aiming to understand the well-being of older, community-dwelling Americans by examining the interactions among physical health, illness, medication use, cognitive function, emotional health, sensory function, health behaviors, and social connectedness. It is designed to provide health providers, policy makers, and individuals with useful information and insights into these factors, particularly on social and intimate relationships.

The National Opinion Research Center (NORC), along with Principal Investigators at the University of Chicago, conducted more than 3,000 interviews during 2005 and 2006 with a nationally representative sample of adults aged 57 to 85. Face-to-face interviews and biomeasure collection took place in respondents' homes. Round 2 interviews were conducted from August 2010 through May 2011, during which Round 1 Respondents were re-interviewed. An attempt was also made to interview individuals who were sampled in Round 1 but declined to participate. In addition, spouses or co-resident partners were also interviewed using the same instruments as the main respondents. This process resulted in 3,377 total respondents. The following files constitute Round 2: Core Data, Disposition of Round 1 Partner Data, Social Networks Data, Social Networks Update Data, Partner History Data, Partner History Update Data, Medications Data, Proxy Data, and Sleep Statistics Data.

Included in the Core files (Datasets 1 and 2) are demographic characteristics, such as gender, age, education, race, and ethnicity. Other topics covered respondents' social networks, social and cultural activity, physical and mental health including cognition, well-being, illness, history of sexual and intimate partnerships, and patient-physician communication, in addition to bereavement items. Data were also collected from respondents on the following items and modules: social activity items, physical contact module, sexual interest module, get up and go assessment of physical function, and a panel of biomeasures, including weight, waist circumference, height, blood pressure, smell, saliva collection, and taste.

The Disposition of Round 1 Partner files (Datasets 3 and 4) detail information derived from Section 6A items regarding the partner from Round 1 within the questionnaire. This provides a complete history for respondent partners across both rounds.

The Social Networks files (Datasets 5 and 6) contain one record for each person identified on the network roster. Respondents who refused to participate in the roster or who did not identify anyone are not represented in this file.

The Social Networks Update files (Datasets 7 and 8) detail respondents' current relationship status with each person identified on the network roster.

The Partner History file (Dataset 9) contains one record for each marriage, cohabitation, or romantic relationship identified in Section 6A of the questionnaire, including a current partner in Round 2 but excluding the partner from Round 1.

The Partner History Update file (Dataset 10) details respondents' current sexual partner information, as well as marital and cohabiting status.

The Medications Data file (Dataset 11) contains records for items listed in the medications log.

The Proxy Data files (Datasets 12 and 13) contain information from proxy interviews administered for Round 1 Respondents who were either deceased or whose health was too poor to participate in Round 2.

The Sleep Statistics Data files (Dataset 14 and 15) provide information on actigraphy sleep variables.

NACDA also maintains a Colectica portal with the NSHAP Core data across rounds 1-3, which allows users to interact with variables across rounds and create customized subsets. Registration is required.

The National Social Life, Health and Aging Project (NSHAP) is a population-based study of health and social factors on a national scale, aiming to understand the well-being of older, community-dwelling Americans by examining the interactions among physical health, illness, medication use, cognitive function, emotional health, sensory function, health behaviors, and social connectedness. It is designed to provide health providers, policy makers, and individuals with useful information and insights into these factors, particularly on social and intimate relationships.

The National Opinion Research Center (NORC), along with Principal Investigators at the University of Chicago, conducted more than 3,000 interviews during 2005 and 2006 with a nationally representative sample of adults aged 57 to 85. Face-to-face interviews and biomeasure collection took place in respondents' homes. Round 3 was conducted from September 2015 through November 2016, where 2,409 surviving Round 2 respondents were re-interviewed, and a New Cohort consisting of adults born between 1948 and 1965 together with their spouses or co-resident partners was added. All together, 4,777 respondents were interviewed in Round 3. The following files constitute Round 3: Core Data, Social Networks Data, Disposition of Returning Respondent Partner Data, and Proxy Data.

Included in the Core files (Datasets 1 and 2) are demographic characteristics, such as gender, age, education, race, and ethnicity. Other topics covered respondents' social networks, social and cultural activity, physical and mental health including cognition, well-being, illness, history of sexual and intimate partnerships and patient-physician communication, in addition to bereavement items. In addition data on a panel of biomeasures including, weight, waist circumference, height, and blood pressure was collected. The Social Networks (Datasets 3 and 4) files detail respondents' current relationship status with each person identified on the network roster. The Disposition of Returning Respondent Partner (Datasets 5 and 6) files detail information derived from Section 6A items regarding the partner from Rounds 1 and 2 within the questionnaire. This provides a complete history for respondent partners across both rounds. The Proxy (Datasets 7 and 8) files contain final health data for Round 1 and Round 2 respondents who could not participate in NSHAP due to disability or death.

The COVID-19 sub-study, administered to NSHAP R3 respondents in the Fall of 2020, was a brief self-report questionnaire that probed how the coronavirus pandemic changed older adults' lives. The COVID-19 sub-study questionnaire was limited to assessing specific domains in which respondents may have been affected by the coronavirus pandemic, including: (1) COVID experiences, (2) health and health care, (3) job and finances, (4) social support, (5) marital status and relationship quality, (6) social activity and engagement, (7) living arrangements, (8) household composition and size, (9) mental health, (10) elder mistreatment, (11) health behaviors, and (12) positive impacts of the coronavirus pandemic. Questions about engagement in racial justice issues since the death of George Floyd in police custody were also added to facilitate analysis of the independent and compounding effects of both the COVID-19 pandemic and reckoning with longstanding racial injustice in America.