Search results

Showing 1 – 20 of 20 results.
Curated
Partially restricted
Simple Crosstabs

Americans' Changing Lives: Waves I, II, III, IV, V, and VI, 1986, 1989, 1994, 2002, 2011, and 2021 (ICPSR 4690)

Released/updated on: 2024-12-12
Geographic coverage: United States
Time period: 1986-01-01--2021-12-31

The Americans' Changing Lives (ACL) survey series is an ongoing, nationally representative, longitudinal study focusing especially on differences between Black and White Americans in middle and late life. These data constitute the first, second, third, fourth, fifth, and sixth waves in a panel survey covering a wide range of sociological, psychological, mental, and physical health items. Wave I of the study began in 1986 with a nation face-to-face survey of 3,617 adults ages 25 and up, with Black Americans and people aged 60 and over over-sampled at twice the rate of the others. Wave II constitutes face-to-face re-interviews in 1989 of those still alive. Survivors have been re-interviewed by telephone, and when necessary face-to-face, in 1994 (Wave III), 2001/02 (Wave IV), 2011 (Wave V), and 2019/21 (Wave VI).

Please note that for Wave VI, the majority of data collection occurred in 2019, with only a small subset (n=39) of participants surveyed in 2021.

ACL was designed and sought to investigate the following: (1) The ways in which a wide range of activities and social relationships that people engage in are broadly "productive," (2) how individuals adapt to acute life events and chronic stresses that threaten the maintenance of health, effective functioning, and productive activity, and (3) sociocultural variations in the nature, meaning, determinants, and consequences of productive activity and relationships. Among the topics covered are interpersonal relationships (spouse/partner, children, parents, friends), sources and levels of satisfaction, social interactions and leisure activities, traumatic life events (physical assault, serious illness, divorce, death of a loved one, financial or legal problems), perceptions of retirement, health behaviors (smoking, alcohol consumption, overweight, rest), and utilization of health care services (doctor visits, hospitalization, nursing home institutionalization, bed days). Also included are measures of physical health, psychological well-being, and indices referring to cognitive functioning.

Demographic information provided for individuals includes household composition, number of children and grandchildren, employment status, occupation and work history, income, family financial situation, religious beliefs and practices, ethnicity, race, education, sex, and region of residence.

Curated

Detroit Area Study, 1985: Life Events in Everyday Experience (ICPSR 6414)

Released/updated on: 2010-08-20
Geographic coverage: Detroit, United States, Michigan
Time period: 1985-01-01--1985-12-31

The 1985 Detroit Area Study surveyed life events of respondents. Questions addressed alcohol and drug use, emotional state, incidents of depression and fear, stress caused by children and work, and respondent's general health. Information on the respondent's family background was also collected, with specific emphases on children, parenting, and marriage. Gender comparison questions were posed to explore in detail issues such as the benefits/responsibilities of marriage, marriage roles and careers, and division of housework tasks. The survey also included items on the respondent's financial situation, social life, social support network, and demographic characteristics such as age, race, sex, education, religion, and income.

Curated

Detroit Area Study, 1995: Social Influence on Health: Stress, Racism, and Health Protective Resources (ICPSR 3272)

Released/updated on: 2002-08-16
Geographic coverage: Detroit, United States, Michigan
Time period: 1995-01-01--1995-12-31

This survey explored the ways in which social influences, such as stress and racism, affected health, and the impact these influences had on the respondents' outlook on life. Respondents were questioned about their health status and their exercise, smoking, sleeping, and dieting habits, as well as about diagnosed health problems and depression and their effects on daily activities. Respondents were also asked a series of questions regarding their employment status, type of job and whether it was a supervisory position, the racial makeup of their workgroup, their perceptions of their position and job, the likelihood of their finding another job, hassles experienced while at work, and whether they had any trouble balancing family and work. Another series of questions asked respondents whether they had been a victim of a serious physical attack or assault, robbery, or home burglary, if they had ever been unfairly searched, stopped, or questioned by police, why they felt they had been treated this way, and if they felt they had ever been treated unfairly by a teacher, landlord, or neighbor. Opinions were also solicited on the respondents' experience with depression and anxiety. Respondents were asked whether they felt it was possible to reach their goals, how satisfied they were with their present situation, how often they felt depressed and how long this feeling lasted, whether they lost weight or sleep due to this feeling, how this feeling of depression made them view themselves, how often and how long they were worried about things that were not likely to happen, how often they worried about non-serious things, and how they felt physically when they were anxious or depressed. Another set of questions queried respondents on alcohol and drug use. Respondents were asked how often they drank alcohol, the most they had to drink at one time, whether they had experienced any addiction to alcohol or experienced any emotional or psychological problems associated with drinking, whether they had any problem controlling their drinking, whether they had used drugs outside of a doctor's order, what types of drugs they had used, how often and in what type of situations they had used these drugs, and whether they had any addiction to the drugs. Respondents were also asked whether they had a regular doctor, whether they went to a doctor's office or clinic to seek medical attention, the last time they had gone for a checkup, how they were treated by staff at the visit, whether they trusted their doctor, the reasons why they did or did not receive medical attention, and whether they had health insurance. Respondents were also asked for their perceptions of differences between Blacks and whites, attitudes toward affirmative action with regard to employment, and their attitude toward interracial relationships. Another battery of questions queried respondents on any fears or phobias they had, such as a fear of animals, water, or visiting a doctor or dentist. Questions focused on the severity of these fears, how long they had had these fears, and how much these fears interfered in daily activities. A final set of questions gathered demographic information on respondents such as highest level of education completed, political affiliation, religious affiliation, level of religious participation, importance of religion, birth date, whether they owned their own home or rented, how much they spent on food each week, total family income for the year 1994, and the height and weight of respondents.

Curated

Mental Health Concerns of Gay and Bisexual Men Seeking Mental Health Services, 2000 [United States] (ICPSR 22121)

Released/updated on: 2010-06-17
Geographic coverage: United States, New England
Time period: 2000-01-01--2000-06-30
This retrospective chart review was conducted on gay and bisexual men who presented for a mental health intake at a health center between January 2000 and June 2000 during which time intake procedures and assessments remained the same. Mental health intakes consisted of one- to three-hour clinical interviews conducted by psychologists and clinical social workers, who determined treatment recommendations and assignments. Current presenting problem(s) and history of them; prior medical, mental health and substance abuse treatment; current symptoms; areas of impaired functioning; and abuse history were included. Because mental health is a key component of overall quality of life, mental health providers who work with MSM can use these data to increase awareness of the types of mental concerns that are most distressing to this population.
Curated
Restricted

Midlife in the United States (MIDUS 2): Milwaukee African American Sample, 2005-2006 (ICPSR 22840)

Released/updated on: 2024-02-26
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2005-01-01--2006-12-31
As a refinement to Midlife in the United States (MIDUS 2), 2004-2006 (ICPSR 4652), a sample of African Americans from Milwaukee was included to examine health issues in minority populations. Areas of the city of Milwaukee, Wisconsin, were stratified according to the proportion of the population that were African American. Those areas with high concentrations were sampled at higher rates than areas with lower concentrations. Area probability sampling methods were used along with population counts from the 2000 United States Census to identify potential respondents. Field interviewers screened households to determine if they contained any African American adults. There was additional screening to achieve an appropriate age/gender distribution in a manner similar to what was done for the original MIDUS sample Midlife in the United States (MIDUS 1), 1995-1996 (ICPSR 2760). Milwaukee respondents were interviewed in their homes using a Computer Assisted Personal Interview (CAPI) protocol and afterwards asked to complete a Self-Administered Questionnaire (SAQ). All measures paralleled those used in the larger MIDUS 1 and 2 samples. After successful completion of the Project 1 survey, some participants were eligible to participate in other MIDUS projects (2 through 5). Survey data was collected for 592 individuals.
Curated
Restricted

Midlife in the United States (MIDUS 3): Milwaukee African American Sample, 2016-2017 (ICPSR 37120)

Released/updated on: 2026-07-20
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2016-01-01--2017-12-31

In 2005, 592 African Americans from Milwaukee were added to the MIDUS sample to examine health issues in minority populations (for more details, see Midlife in the United States (MIDUS 2): Milwaukee African American Sample [ICPSR #22840]). Respondents were interviewed in their homes using a Computer Assisted Personal Interview (CAPI) survey protocol and asked to complete and return a Self-Administered Questionnaire (SAQ). Afterwards these individuals were eligible for participation in the same research protocol as the national MIDUS 2 sample, including cognitive, daily stress, biomarker, and neuroscience projects.

With support from the National Institute on Aging, a second wave of survey data collection on the Milwaukee sample was begun in 2016. The survey consisted of a 2.5 hour CAPI interview followed by a 45-page mailed SAQ. CAPI survey data was collected for 389 individuals, realizing a 78 percent response rate, adjusted for mortality and other eligibility criteria. Data collection for this follow-up wave largely repeated baseline assessments, with additional questions in selected areas (e.g., economic recession experiences, childhood experience with race, etc.). Following successful completion of the CAPI and SAQ protocols, individuals were eligible for participation in cognitive, daily stress, biomarker, and neuroscience projects.

Curated
Restricted

Midlife in the United States (MIDUS Refresher 1): Milwaukee African American Sample, 2012-2013 (ICPSR 36722)

Released/updated on: 2025-09-11
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2012-01-01--2013-12-31

In 2012-2013, the MIDUS Milwaukee Refresher study recruited a sample of 508 Milwaukee African American adults, aged 25 to 64, designed to replenish the Midlife Development in the United States (MIDUS 2): Milwaukee African American Sample, 2005-2006 (ICPSR 22840). This sample was also designed to increase the number of racial minorities included in the broader MIDUS study. The MIDUS Milwaukee Refresher survey employed the same assessments (demographic, psycho-social, and physical and mental health) as those assembled on the existing MIDUS sample, but with additional questions about the effect of the economic recession of 2008-09. A sample of African Americans from Milwaukee County, Wisconsin, was stratified by age, gender, and income.

Area probability sampling methods were used to identify potential respondents. Field interviewers screened households to determine if they contained any African American adults. There was additional screening to achieve an appropriate age/gender distribution in a manner similar to what was done for the original MIDUS sample (Midlife in the United States (MIDUS 1), 1995-1996 [ICPSR 2760]). Milwaukee respondents were interviewed in their homes using a 2.5-hour Computer Assisted Personal Interview (CAPI) protocol and afterwards asked to complete a self-administered questionnaire (SAQ). All measures paralleled those used in the larger MIDUS samples. In addition to successful completion of the survey, participants were asked to complete a cognitive assessment by phone. Some respondents were eligible to participate in additional MIDUS projects: daily diary assessments, biomarker assessments, and neuroscience assessments.

Curated
Restricted

Midlife in the United States (MIDUS Refresher 2): Milwaukee African American Sample, 2023-2024 (ICPSR 39583)

Released/updated on: 2025-11-19
Geographic coverage: Milwaukee, United States, Wisconsin
Time period: 2023-01-01--2024-12-31

In 2012-2013, the MIDUS Milwaukee Refresher study recruited a sample of 508 Milwaukee African American adults, aged 25 to 64, designed to replenish the original MIDUS Milwaukee 1 survey that was designed to increase the number of racial minorities in 2005. The MIDUS Milwaukee Refresher survey employed the same comprehensive assessments (demographic, psycho-social, and physical and mental health) as those on the existing MIDUS sample, with additional questions about the effect of the Great Recession in 2008-09.

In 2023-2024, the second wave of survey data was collected from 327 longitudinal Refresher Milwaukee participants, including the questions (1) repeated from the Refresher 1, (2) new impacts of the COVID-19 pandemic replacing the questions related to the Great Recession in the Refresher 1, and (3) the additional questions in selected areas (e.g., AD8, IADL, family history of dementia). This new longitudinal MIDUS Refresher Milwaukee data allow examination of period effects on health and well-being related to the COVID-19 pandemic by comparing the pre-pandemic MIDUS Refresher Milwaukee 1 data with the post-pandemic MIDUS Refresher Milwaukee 2 data. Further, the longitudinal MIDUS Refresher datasets (wave 1 and wave 2) allow investigation of the two major macro-level historic events, the Great Recession and the COVID-19 pandemic, on health and well-being.

Curated
Simple Crosstabs

Midlife in the United States (MIDUS): Survey of Minority Groups [Chicago and New York City], 1995-1996 (ICPSR 2856)

Released/updated on: 2018-03-21
Geographic coverage: New York City, United States, Chicago, Illinois, New York (state)
Time period: 1995-01-01--1996-12-31
This survey of minority groups was part of a larger project to investigate the patterns, predictors, and consequences of midlife development in the areas of physical health, psychological well-being, and social responsibility. Conducted in Chicago and New York City, the survey was designed to assess the well-being of middle-aged, urban, ethnic minority adults living in both hyper-segregated neighborhoods and in areas with lower concentrations of minorities. Respondents' views were sought on issues relevant to quality of life, including health, childhood and family background, religion, race and ethnicity, personal beliefs, work experiences, marital and close relationships, financial situation, children, community involvement, and neighborhood characteristics. Questions on health explored the respondents' physical and emotional well-being, past and future attitudes toward health, physical limitations, energy level and appetite, amount of time spent worrying about health, and physical reactions to those worries. Questions about childhood and family background elicited information on family structure, the role of the parents with regard to child rearing, parental education, employment status, and supervisory responsibilities at work, the family financial situation including experiences with the welfare system, relationships with siblings, and whether as a child the respondent slept in the same bed as a parent or adult relative. Questions on religion covered religious preference, whether it is good to explore different religious teachings, and the role of religion in daily decision-making. Questions about race and ethnicity investigated respondents' backgrounds and experiences as minorities, including whether respondents preferred to be with people of the same racial group, how important they thought it was to marry within one's racial or ethnic group, citizenship, reasons for moving to the United States and the challenges faced since their arrival, their native language, how they would rate the work ethic of certain ethnic groups, their views on race relations, and their experiences with discrimination. Questions on personal beliefs probed for respondents' satisfaction with life and confidence in their opinions. Respondents were asked whether they had control over changing their life or their personality, and what age they viewed as the ideal age. They also rated people in their late 20s in the areas of physical health, contribution to the welfare and well-being of others, marriage and close relationships, relationships with their children, work situation, and financial situation. Questions on work experiences covered respondents' employment status, employment history, future employment goals, number of hours worked weekly, number of nights away from home due to work, exposure to the risk of accident or injury, relationships with coworkers and supervisors, work-related stress, and experience with discrimination in the workplace. A series of questions was posed on marriage and close relationships, including marital status, quality and length of relationships, whether the respondent had control over his or her relationships, and spouse/partner's education, physical and mental health, employment status, and work schedule. Questions on finance explored respondents' financial situation, financial planning, household income, retirement plans, insurance coverage, and whether the household had enough money. Questions on children included the number of children in the household, quality of respondents' relationships with their children, prospects for their children's future, child care coverage, and whether respondents had changed their work schedules to accommodate a child's illness. Additional topics focused on children's identification with their culture, their relationships with friends of different backgrounds, and their experiences with racism. Community involvement was another area of investigation, with items on respondents' role in child-rearing, participation on a jury, voting behavior, involvement in charitable organizations, volunteer experiences, whether they made monetary or clothing donations, and experiences living in an institutional setting or being homeless. Respondents were also queried about their neighborhoods, with items on neighborhood problems including racism, vandalism, crime, drugs, poor schools, teenage pregnancy, the existence of social networks, the frequency of contact with family members, social interaction with neighbors, sense of community, whether the respondent owned or rented their home, and the financial, legal, and medical problems of family members. A final set of questions sought respondents' assessments of their life and their expectations for the future. Additional background information on respondents includes age, ethnicity, and gender.
Curated

National Survey of Black Americans, 1979-1980 (ICPSR 8512)

Released/updated on: 2005-11-04
Geographic coverage: United States
Time period: 1979-01-01--1980-12-31
The purpose of this data collection is to provide an appropriate theoretical and empirical approach to concepts, measures, and methods in the study of Black Americans. The questionnaire was developed over two years, with input from social scientists, students, and a national advisory panel of Black scholars. The final instrument encompasses several broad areas related to Black American life. The study explores neighborhood-community integration, services, crime and community contact, the role of religion and the church, physical and mental health, and self-esteem. It also examines employment, the effects of chronic unemployment, the effects of race on the job, and interaction with family and friends. In addition, the survey provides information on racial attitudes, race identity, group stereotypes, and race ideology. Demographic variables include education, income, occupation, and political behavior and affiliation.
Curated

National Survey of Black Americans, Waves 1-4, 1979-1980, 1987-1988, 1988-1989, 1992 (ICPSR 6668)

Released/updated on: 2005-11-04
Geographic coverage: United States
The purpose of this data collection was to provide an appropriate theoretical and empirical approach to concepts, measures, and methods in the study of Black Americans. Developed with input from social scientists, students, and a national advisory panel of Black scholars, the survey investigates neighborhood-community integration, services, crime and community contact, the role of religion and the church, physical and mental health, self-esteem, life satisfaction, employment, the effects of chronic unemployment, the effects of race on the job, interaction with family and friends, racial attitudes, race identity, group stereotypes, and race ideology. Demographic variables include education, marital status, income, employment status, occupation, and political behavior and affiliation.
Curated
Simple Crosstabs

National Survey of Families and Households, Wave 1: 1987-1988, [United States] (ICPSR 6041)

Released/updated on: 2017-08-31
Geographic coverage: United States
Time period: 1987-03-01--1988-05-31

The National Survey of Families and Households (NSFH), Wave 1 (1987-1988) is the first of three waves in a longitudinal survey that was designed to study the causes and consequences of changes happening in families and households within the United States. At a time when the range of family structures was becoming more and more diverse, this study permitted a close examination of the resulting family compositions and household operations. One adult per household was randomly selected as the primary respondent, and there was a total of 13,007 respondents. In addition to the main interview conducted with the primary respondent, a shorter, self-administered questionnaire was given to the spouse or cohabitating partner, and also administered to the householder if he or she was a relative of the primary respondent.

A considerable amount of life-history information was collected, such as the respondent's family living arrangements in childhood, departures and returns to the parental home, and histories of marriage, separation, divorce, cohabitation, adoption, child custody arrangements, and stepfamily relations. Respondents were also asked about the relationship of household members to each other and the quality of their relationships with their parents, children, and in-laws. Information on economic well-being was also collected, including earnings from wages, self-employment income, interest, dividends, investments, pensions, Social Security, public assistance, and child support/alimony. Demographic information collected includes sex, age, marital status, education, and employment.

Curated
Simple Crosstabs

National Survey of Families and Households, Wave 2: 1992-1994, [United States] (ICPSR 6906)

Released/updated on: 2018-06-06
Geographic coverage: United States
Time period: 1992-07-01--1994-08-31

The National Survey of Families and Households (NSFH), Wave 2 1992-1994, a longitudinal population-based survey of families and households in the United States, investigates the causes and consequences of changes in American family and household structure. This is the second wave of a three part survey. The current study, NSFH Wave 2, is the second follow up and was conducted in 1992-1994. The sample included all NSFH Wave 1 main respondents and spouse/partner with focal children and all other NSFH Wave 1 main respondents ages 45 and over in 2000, as well as their NSFH Wave 1 spouse/partner.

The Wave 2 survey included the following components: (1) an interview of all surviving members of the original sample via face-to-face personal interview, (2) a personal interview with the current spouse or cohabiting partner almost identical to the interview with the main respondent, (3) a personal interview with the original spouse or partner of the primary respondent in cases where this relationship had ended, (4) a telephone interview with "focal children" who were originally aged 13-18 in Wave 1, (5) a short telephone interview with "focal children" who were originally aged 5-12 in Wave 1, (6) short proxy interviews with a surviving spouse or other relative in cases where the original respondent had died or was too ill to interview, and (7) a telephone interview with a randomly-selected parent of the main respondent. Demographic information collected includes sex, age, marital status, education, and employment

Curated
Simple Crosstabs

National Survey of Families and Households, Wave 3: 2001-2003, [United States] (ICPSR 171)

Released/updated on: 2018-06-06
Geographic coverage: United States
Time period: 2001-01-01--2003-12-31
The National Survey of Families and Households (NSFH) is a longitudinal population-based survey series that seeks to examine the causes and consequences of change in American family and household structures. NSFH Wave 3 was conducted in 2001-2003 and represents the third follow-up survey. The Wave 3 sample included interviews with all NSFH Wave 1 main respondents and spouse/partner with a focal child eligible for the NSFH Wave 2 interviews, interviews with these focal children (now aged 18-34), and interviews with all other NSFH Wave 1 main respondents aged 45 and over in the year 2000, as well as their NSFH Wave 1 spouse/partner.
Curated

Quality of American Life, 1971 (ICPSR 3508)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1971-01-01--1971-12-31
The purpose of this study was to survey Americans about perceived quality of life by measuring perceptions of their socio-psychological condition, their needs and expectations from life, and the degree to which those needs were satisfied. The data were collected via personal interviews from a nationwide probability sample of 2,164 persons 18 years of age and older during the summer of 1971. Closed and open-ended questions were used to probe respondents' satisfactions, dissatisfactions, aspirations, and disappointments in a variety of life domains, such as dwelling/neighborhood, local services (e.g., police, roads, and schools), public transportation, present personal life, life in the United States, education, occupation, job history/expectation, work life, housework, leisure activities, organizational affiliations, religious affiliation, health problems, financial situation, marriage (including widowhood, divorce, and separation), children/family life, and relationships with family and friends. In addition to broad questions about satisfaction with each of these domains and their importance to the respondents, specific sources of gratification and frustration are explored. Other questions focused on life as a whole and the extent to which respondents felt they had control over their lives (e.g., rating of various aspects of life, (dis)satisfaction with life, personal efficacy, and social desirability measures). Personal data include sex, age, race, ethnic background, childhood family stability, military service, and father's occupation and education. Observational data are included on housing and neighborhood characteristics as well as respondents' appearance, intelligence, and sincerity. An instructional subset of this study is also available (see ICPSR INSTRUCTIONAL SUBSET: QUALITY OF AMERICAN LIFE, 1971 [ICPSR 7516], also prepared by Campbell, Converse, and Rodgers.) It includes questions representative of the major areas covered in the original, longer survey. A related dataset, QUALITY OF AMERICAN LIFE, 1978 (ICPSR 7762), continues the survey conducted in 1971.
Curated

Quality of American Life, 1978 (ICPSR 7762)

Released/updated on: 1992-02-16
Geographic coverage: United States
Time period: 1978-01-01--1978-12-31
This dataset is a continuation of one created seven years earlier, QUALITY OF AMERICAN LIFE, 1971 (ICPSR 3508). In the 1978 study, a national sample was drawn that included many respondents from the 1971 study. The purpose of the study was to survey Americans about their perceived quality of life by measuring their perceptions of their socio-psychological condition, their needs and expectations from life, and the degree to which those needs were satisfied. The data, similar in scope and content of that in the 1971 survey, were collected via personal interviews from a nationwide probability sample of 3,692 persons 18 years of age and older during the summer of 1978. Closed and open-ended questions were used to probe respondents' satisfactions, dissatisfactions, aspirations, and disappointments in a variety of life domains, such as dwelling/neighborhood, local services (e.g., police, roads, and schools), public transportation, present personal life, life in the United States, education, occupation, job history/expectation, work life, housework, leisure activities, organizational affiliations, religious affiliation, health problems, financial situation, marriage (including widowhood, divorce, and separation), children/family life, and relationships with family and friends. In addition to broad questions about satisfaction with each of these domains and their importance to the respondents, specific sources of gratification and frustration were explored. Other questions focused on life as a whole and about the extent to which respondents felt they had control over their lives (e.g., rating of various aspects of life, (dis)satisfaction with life, personal efficacy, and social desirability measures). A major difference between this study and the earlier study is that the 1978 respondents were asked more detailed questions concerning their perceived financial status relative to their family, friends, and past personal financial status. Personal data include sex, age, race, ethnic background, childhood family stability, military service, and father's occupation and education. Observational data are included on housing and neighborhood characteristics as well as respondents' appearance, intelligence, and sincerity.
Curated

Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001, Baseline and Follow-Up Data (ICPSR 3678)

Released/updated on: 2006-09-26
Geographic coverage: United States, Tennessee, California, Alabama, Florida, Birmingham, Pennsylvania, Miami, Palo Alto, Massachusetts, Memphis, Philadelphia, Boston
Time period: 1996-09-01--2001-02-28
Resources for Enhancing Alzheimer's Caregiver Health (REACH) was established in 1995 to conduct social and behavioral research on interventions designed to enhance family caregiving, particularly in minority families, for persons with Alzheimer's Disease and related disorders. Baseline data (ICPSR 3253) were collected through randomized clinical trials at six sites: University of Alabama-Birmingham, The Research and Training Institute of the Hebrew Rehabilitation Center for Aged in Boston, University of Tennessee-Memphis, University of Miami, Veterans Affairs Palo Alto Health Care System and Stanford University, and Thomas Jefferson University in Philadelphia. Interventions such as psychoeducational support groups, behavioral skills training programs, family-based systems interventions, environmental modifications, and technological computer-based information and communication services varied by site. This collection contains baseline data along with follow-up data at 6-, 12-, and 18-month intervals from each site with focus on the impact of the various intervention strategies on psychological distress, health status, health practices, and health care utilization. Also included are follow-up batteries, transition batteries (placement, bereavement, discontinued), and data reporting missed visits. Parts 1 through 5 contain screening data and responses to a short mental status questionnaire. Parts 6 through 34 contain baseline data along with follow-up data at 6, 12, and 18-month intervals and cover activities of daily living, anxiety, and caregiver health and health behaviors along with sociodemographic information. Also included are care recipient medications and sociodemographic information. Parts 35 through 40 contain tracking data and also include an examination of interventions.
Curated

Resources for Enhancing Alzheimer's Caregiver Health (REACH II), 2001-2004 (ICPSR 4354)

Released/updated on: 2006-10-27
Geographic coverage: Palo Alto, United States, Tennessee, Memphis, California, Alabama, Florida, Birmingham, Philadelphia, Pennsylvania, Miami
Time period: 2001-01-01--2004-12-31
Built upon the findings of RESOURCES FOR ENHANCING ALZHEIMER'S CAREGIVER HEALTH, 1996-2001, BASELINE AND FOLLOW-UP DATA [ICPSR 3678], REACH II designed and tested a single multi-component intervention among family caregivers of persons with Alzheimer's disease or related disorders. The overall objectives were (1) to identify and reduce modifiable risk factors among diverse family caregivers of patients with Alzheimer's Disease or a related disorder, (2) to enhance the quality of care provided to the care recipients, and (3) to enhance the well-being of the caregivers. REACH II is the first project to simultaneously test a comprehensive caregiver intervention in three distinct racial/ethnic groups: Hispanic/Latino, Black/African-American, and White/Caucasian. The intervention was based on a risk-appraisal approach in which five areas of risk--depression, burden, self-care, social support, and patient problem behaviors--that are central to caregiver well-being and quality of life were matched to corresponding intervention components. These components included education, skills to manage troublesome care-recipient behaviors, social support, cognitive strategies for reframing negative emotional responses, and strategies for enhancing healthy behaviors and managing stress. Consistent with this approach, the primary outcome was a multivariate quality of life indicator that assessed caregiver depression, burden, self-care, social support, and patient problem behaviors. Two hallmarks of caregiver intervention studies--caregiver clinical depression and patient institutionalization--were assessed as secondary outcomes. The dataset names listed in this collection include the shortened name of the form administered.
Curated
Simple Crosstabs

Stroke Recovery in Underserved Populations 2005-2006 [United States] (ICPSR 36422)

Released/updated on: 2016-05-03
Geographic coverage: United States
Time period: 2005-01-01--2006-12-31

The Stroke Recovery in Underserved Populations 2005-2006 study was created to address the National Institute on Aging (NIA) Request For Application entitled "Research on Mind-Body Interactions and Health" (RFA OD-03-008). It addressed the NIA interest in "the impact of optimism, happiness, or a positive attitude on well-being and health; and social functioning and health." The study examined how positive emotion (e.g., joy, gratitude, love, contentment) and social networks independently and interactively contribute to recovery of functional status after stroke within two underserved groups. The specific study aims were to:

  1. Examine recovery of functional status (motor and cognitive function), for White, African American and Hispanic persons with stroke discharged from rehabilitation facilities
  2. Examine the contributions of positive emotion and social networks on recovery of functional status (motor and cognitive function), for White, African American, and Hispanic persons with stroke discharged from rehabilitation facilities; and
  3. Examine the interaction between positive emotion and social networks on recovery of functional status (motor and cognitive function) for White, African American, and Hispanic persons with stroke discharged from rehabilitation facilities.

The data were collected by the IT Health Track at four time points: at admission and discharge from rehabilitation facility, and 80-180 days and 365-425 days after discharge. These data emphasize recovery of motor and cognitive functional status, positive emotion, and social networks

The dataset contains 226 variables and 1219 cases from 11 rehabilitation facilities across the United States.

Curated

Women's Health in Boston and Cambridge, 2000 [Massachusetts] (ICPSR 26583)

Released/updated on: 2010-06-16
Geographic coverage: United States, Massachusetts, Cambridge, Boston
Time period: 2000-09-01--2000-11-30
Using Random Digit Dial, this study tested the feasibility of using a brief telephone interview to assess sexual attraction, behavior, and identity among women. A neighborhood in Boston with a high density of lesbian residents was selected. The study used three criteria to identify a neighborhood that was expected to have a high density of lesbian residents. Neighborhoods were defined by a postal ZIP code so that potential respondents could easily identify whether or not they lived in the target area. The criteria used were: (a) a high proportion of never-married females aged 35 years or older (calculated as ratio of ZIP code area to city wide, United States Department of Commerce, 1990), (b) a high proportion of female-headed households who also reported an unmarried female partner in the household (United States Department of Commerce, Bureau of the Census, 1990), and (c) a high proportion of female patients from the ZIP code area among Fenway Community Health Center female patients (Fenway Community Health Center is a major health service provider to gay and lesbian populations in Boston and Cambridge). These criteria led to the selection of the Jamaica Plain neighborhood in Boston. Women were eligible if they resided in that area, were between the ages of 18 and 59 years, and spoke English well enough to be able to answer the interview questions. Phone interviews lasted a mean of 5.6 minutes. Respondents who identified themselves as lesbian or bisexual completed an additional specialized section that lasted a mean of 2.5 minutes and inquired about participation in and identification with the gay/lesbian community. In total, 1,250 numbers were dialed. Of them, 169 (14 percent) were nonworking numbers, 165 (13 percent) were not households (e.g., businesses), 235 (19 percent) were indeterminable (number was never answered by a person), and 681 (54 percent) were households. Of these households, 439 (64 percent) were successfully screened, 176 (26 percent) refused or delayed screening, and 66 (10 percent) could not be screened (e.g., language barriers). Of the screened households, 223 (51 percent) were not eligible. Of 216 eligible households, 202 (94 percent) women completed the interview.
Back to top