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Showing 1 – 30 of 30 results.

Curated

Public Health Law Research Distracted Driving Laws Dataset, 2000-2011 (ICPSR 34551)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 2000-01-01--2011-01-01

This project compiled state and District of Columbia laws regulating the use of mobile communication devices (MCD) by individuals operating motor vehicles and coded some of the laws' features in a data file.

The data file contains information about prohibitions against talking or texting on a MCD for different groups of drivers:

16 year old drivers with provisional or beginner licenses
All 16 year old drivers
17 year old drivers with provisional or beginner licenses
All 17 year old drivers
18 year old drivers with provisional or beginner licenses
All 18 year old drivers
All drivers with provisional or beginner licenses
All drivers

For each of these groups, the coded features include the date each provision against talking or texting on a MCD went into effect, whether there is hands-free exception to the prohibition, whether there is a primary or secondary method of enforcement, and the minimum and maximum fines for the first, second, and third violations. The data file is structured so that each record reflects the coded features of relevant law at a given month. Thus, every state and the District of Columbia has 144 records in the file, one for each month from January 2000 to December 2011.

A separate PDF file contains the text of the laws.

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State Pre-Emption of Municipal Laws and Policies Affecting Immigrants' Culture of Health, North Carolina, 2019-2020 (ICPSR 38558)

Released/updated on: 2022-10-10

Geographic coverage: North Carolina, United States

Time period: 2019-08-01--2020-02-29

Municipal laws and policies affect the social, economic, and legal conditions of civic and private lives of immigrants in profound and fundamental ways, including both direct access to health services, as well as broader social determinants that contribute to a Culture of Health, such as employment, housing, education, transportation, and law enforcement. Some municipalities have proclaimed themselves sanctuary cities or counties or have adopted laws and policies that limit local involvement in immigration enforcement or protect immigrants to some substantial extent. However, at least nine states have laws that preempt local municipal protective laws and policies, and more than a dozen other states reportedly are considering similar pre-emption laws. The research team systematically examined the consequences of state preemption of protective municipal laws and policies on the health and well-being of a large and particularly vulnerable community in the United States: the immigrant Latinx/Hispanic community.

Curated

State Vaccination Requirements and Exemption Law Database, 2011 (ICPSR 34486)

Released/updated on: 2024-02-14

Geographic coverage: United States

The primary objective of this project was to prepare a complete and comprehensive database of state laws pertaining to immunization requirements and exemptions. To that end, the LexisNexis Academic search engine was used to search statutory and administrative materials for all 50 states and the District of Columbia, using the search term "immunization" together with other relevant terms. That search retrieved 1,991 laws whose characteristics were coded in the database by project staff. This data collection comprises a data file with the coded information and a ZIP archive which contains 1,991 PDF files with the full text of the laws.

After an initial review, the project staff categorized the retrieved laws into three groups. Group 1 consists of laws not applicable to human immunization, such as laws related to immunity from prosecution, vaccination of animals, and state sovereign immunity. Group 2 comprises laws with provisions related to specific vaccination requirements and exemptions as to which vaccines should be given to whom. Lastly, Group 3 covers vaccination laws without provisions related to specific vaccination requirements or exemptions as to which vaccines should be given to whom, for example, laws with provisions for immunization registries, annual reporting requirements, and access to and financing of vaccines.

The amount and type of information recorded about a law in the data file depends on its group classification. For every law in all three groups, the data file identifies the group, names the PDF file with the text of the law, and names the state to which the law applies. For Group 2 and Group 3, the data file also describes the topics covered by the law, the year it came into effect, and whether or not the law is current or repealed. Additional information for Group 2 describes target populations, target institutions, applicable vaccines, and exemption characteristics. The data file also includes brief textual descriptions of the Group 2 laws.

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Project HealthDesign: Estrellita - An Application for Tracking Observations of Daily Living Related to Preterm Infants, 2011-2012 (ICPSR 36029)

Released/updated on: 2024-02-14

Geographic coverage: Orange County, California

Time period: 2011-01-01--2012-01-01

More than 12 percent of all United States births each year are preterm. To improve the care of these infants, which have an increased risk of serious developmental and chronic health problems, the Estrellita team created a mobile phone application to monitor premature infants and their caregivers. This app allows caregivers to better understand the infant care process and to more easily interact with clinicians about themselves and the care of their infants. Caregivers used the Estrellita app to record their own stress levels and mood and their infants' observations of daily living (ODL) such as baby fussiness, diapering, weight, and bonding activities with the babies. In addition, the app allowed the caregivers to track clinical appointments, review the ODL data, and send and receive text messages from clinicians.

The following results may be significantly less relevant compared to results above.

Curated

State Foodborne Illness Reporting Laws, 2011-2013 (ICPSR 34935)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 2011-01-01--2013-01-01

The primary goal of this project was to create a comprehensive database of all state regulations and legislation that can be used by food safety stakeholders to efficiently analyze relevant foodborne illness-related legislation. To that end, project staff compiled state statutes and regulations pertaining to foodborne illness reporting requirements and coded many of their features in a database. The coded information covers reporting requirements for establishments and healthcare providers; investigation authority over establishments and individuals; enforcement regarding suspected/confirmed foods; protection of patient and business confidentiality; and reporting requirements for illness caused by specific pathogens such as Campylobacter, Clostridium botulinum, Clostridium perfringens, Cryptosporidium, Cyclospora, Listeria monocytogenes, Norovirus, Salmonella (nontyphoidal), Shiga toxin-producing Escherichia coli O157:H7, Shigella, Staphylococcus aureus, Toxoplasma gondii, Vibrio, and Yersinia. Additional information recorded in the data include state population size; state per capita income; state participation in the Foodborne Diseases Surveillance Network (FoodNet), Environmental Health Specialist Network (EHS-Net), and Food Emergency Response Network (FERN); and whether or not the state has a FDA FoodCORE regional program, Food Safety Integrated Center for Excellence (FSICE), or FDA Rapid Response Team (RRT) grant.

This data collection comprises a Microsoft Access database with 44 data tables and the Final Exported Dataset which was derived from the database. The Access database contains a draft of the information in the Final Exported Dataset and some information not included in it. The Final Exported Dataset describes the laws and regulations that were current in 2013. The Access database covers the period 2011-2013.

To facilitate the use of this data collection, every data table in the Access database is also provided as a separate data file (Datasets 3-46). In addition, the codebook includes copies of the data entry forms in the Access database .

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National Evaluation Database for the Partnership for Long-Term Care (PLTC) [California, Connecticut, and Indiana], 1992-1998 (ICPSR 2844)

Released/updated on: 2024-02-14

Geographic coverage: Indiana, United States, Connecticut, California

Time period: 1992-01-01--1998-01-01

These data were collected to evaluate the Partnership for Long-Term Care (PLTC), a project in which the Robert Wood Johnson Foundation awarded grants to four states -- California, Connecticut, Indiana, and New York -- to work with private insurers to create long-term care insurance policies that were more affordable and provided better protection against impoverishment than those generally available. PLTC policies combine private long-term care insurance with special Medicaid eligibility standards that protect assets of the insured once private insurance benefits are exhausted. This collection was extracted from a database compiled from data submitted by three of the PLTC states: California, Connecticut, and Indiana (New York refused participation). It comprises seven parts, which can be linked together using common identifying variables. Part 1, Insured, describes the characteristics of each issued policy and includes variables covering the effective policy date, policy type, elimination periods, maximum benefits, inflation protection mode, and annualized premium, as well as the year of birth, sex, marital status, and state of residence of the insured. Each insured person is represented by one or more records: one record for the initial PLTC policy, plus a separate record for each change to the policy, if any. Part 2, Changes, consists of policy change records used to update the policies in Part 1. Assessments for benefits are recorded in Part 3. This file includes variables on the assessment date, whether the insured met policy criteria at the time of the assessment, disability date, deficiencies in activities of daily living, and MSQ and Folstein test scores. Parts 4-6 describe service payments and utilization: reporting period (quarter), type of service received by the insured, service amount billed, days of service rendered, and amount of remaining benefits (dollars and days). Part 7 contains information on persons denied application to PLTC policies, including date of denial, type and amount of coverage sought, reason for denial, and the sex, year of birth, and marital status of the applicant.

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National Survey of Access to Medical Care, 1982 (ICPSR 8244)

Released/updated on: 2005-11-04

Geographic coverage: United States

The purpose of this study, which served to update information available from previous Center for Health Administration Studies/National Opinion Research Center surveys in 1953, 1958, 1963, 1970, and 1976, was to provide current data on the accessibility of medical care for the United States population. The survey collected information on usual sources of medical care, sources of medical care utilized, problems associated with access to sources of care, satisfaction with medical services received, utilization of medical diagnostic procedures, health insurance coverage, episodes of illness, and other health-related issues. Additional information collected by the survey includes household composition, age, sex, income, race, education, employment status, and occupation.

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Creating a Patient Registry to Facilitate Data Sharing and Encourage Patient-Centered Approaches to Improving Health and Lowering Costs, 2013 (ICPSR 35570)

Released/updated on: 2016-10-05

Geographic coverage: United States, Cincinnati, Ohio

Time period: 2013-09-01--2013-12-01

This interventional pilot study was conducted in a primary care clinic to determine if patients would become more engaged in their own health and ask more questions of their physicians if they were provided data about patients similar to themselves. The study was conducted with 150 patients with a diagnosis of hypertension who had scheduled appointments with one of three participating physicians in the clinic. When they arrived at the clinic for their appointment, the patients were shown de-identified clinical data about similar patients with hypertension on a computer screen, given a printout of this information, and then proceeded to visit their physician. After the physician visit the patients completed a short survey. Their answers to the survey questions are recorded in the data file together with additional information about them, such as age, gender, race, smoking status and comorbidities.

The three participating physicians completed a short survey at the end of the study. The results of that survey are summarized in a table provided with the technical documentation.

Curated

Chronic Illness and Caregiving, 2000: [United States] (ICPSR 3402)

Released/updated on: 2024-02-14

Geographic coverage: United States

The objective of this survey, which interviewed individuals from the general public, chronically ill persons, and informal caregivers, was threefold: (1) to assess public awareness of chronic care issues and the level of support for chronic care policy initiatives, (2) to examine experiences and needs of chronically ill Americans concerning health care and other assistance, and (3) to evaluate experiences and needs of informal caregivers. Questions to the general public addressed awareness of the availability of supportive and housing services for the chronically ill, knowledge about coverage for long-term care, concerns about the future of the chronic care delivery system, support for policy initiatives such as tax credits for the chronically ill and caregivers, and support for a policy that would ensure pharmaceutical coverage in Medicare. Chronically ill interviewees responded to questions about access to and experience with chronic care and other health care services, experiences with and needs for clinical services coordination, experiences with and needs for social supports and interventions, and adjustment skills and knowledge (e.g., what were their needs for learning how to live with chronic conditions). Questions for informal caregivers focused on experiences with caregiving (e.g., for whom they provided care, how many hours they devoted to caregiving per week, and living arrangements), balance between caregiving and other areas of their lives, experiences with and needs for respite care, and availability of social supports for caregivers.

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Local Health Department Infrastructure Study, 1999-2000: [United States] (ICPSR 3185)

Released/updated on: 2024-02-14

Time period: 1999-01-01--2000-01-01

The purpose of this survey was to address the paucity of current data on the United States' local public health infrastructure and to advance understanding of the many ways local public health agencies contribute to keeping the nation's population and environment healthy. The survey collected information on local health department (LHD) characteristics (e.g., type of jurisdiction served, office to which the LHD reported directly, total expenditures, and sources of the LHD's total budget), priority program areas, and public health services provided directly or through contracts with others. Additional data cover LHD workforce composition, staffing needs, workforce training, and partnerships and collaborations with other groups and organizations, such as state or federal agencies, hospitals, HMOs, community health centers, universities, community-based organizations, professional associations, faith communities/churches, and business/private corporations. LHDs also reported on completion of community health assessments and development of community health improvement plans.

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Business Leaders' Views on American Health Care, 1990 (ICPSR 6032)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 1990-07-05--1990-12-17

This survey interviewed business leaders from Fortune 500 companies (chief executive officers, presidents, and chairmen of the board) on health care issues. Its purpose was to assess their views on the need for change in the health care system, the directions that such changes should take, and the role that business should play in the health care system. In addition, respondents were asked if their companies self-insured for insurance benefits or purchased coverage from a health insurance company, if there was an executive-level effort at their companies to decide where they stood on national health policy issues, and if they believed their companies would be able to bring their health costs under control over the next year or two. For each company, the data include information on the number of employees, the percentage of total payroll used for health care benefits, the percentage of sales in health-related business, and the company type (financial services and insurance, sales and diversified services, utilities and transportation, durable goods, nondurable goods, and forestry/mining/petroleum).

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Project HealthDesign: iN Touch - Obese Teens and Young Adults Using Mobile Devices to Track Observations of Daily Living, 2011 (ICPSR 36026)

Released/updated on: 2024-02-14

Geographic coverage: San Francisco, United States, California

This study examined the potential of collecting observations of daily living (ODLs) via mobile devices for youths who are managing obesity and are at risk for depression and anxiety. Leveraging TheCarrott.com (thecarrot.com) utilities and data storage platform, the iN Touch design team developed an application for the iPod Touch that study participants used to record their physical activity, food intake, socialization and mood. Study participants shared this information with their lay health coaches and collaboratively set goals with them. The data file contains the ODL information collected with the iPod Touch application.

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Small Business Benefits Study (SBBS), 1990: [Denver, Flint, Tampa, and Tucson] (ICPSR 6002)

Released/updated on: 1998-04-20

Geographic coverage: Flint, United States, Colorado, Tucson, Denver, Florida, Tampa, Arizona, Michigan

This survey was conducted as part of an evaluation of the Robert Wood Johnson Foundation's Health Care for the Uninsured Program (HCUP), a program whose primary focus was the development and marketing of affordable health insurance products for small businesses. The survey investigated the number and types of small businesses that offered and did not offer insurance, the number and types of employees of small businesses who received and did not receive insurance, and whether the employers and employees participating in HCUP were different from those with other types of insurance or from those with no insurance. In addition, the survey was designed to test several hypotheses: whether employers facing an inelastic demand for their product or a tight labor market would be more likely to offer health insurance to their employees, and whether higher wages substitute for health insurance for certain groups of highly skilled or unionized workers. Firm-level data collected by the survey include number of permanent and temporary employees, employee turnover, fringe benefits offered to full- and part-time employees (e.g., paid vacation, paid sick leave, long-term disability insurance, life insurance, retirement plan, group health insurance), type of business, number of years owner had owned the company, age and legal form of the company, and gross revenue. Extensive information on health insurance was obtained from firms offering this benefit: total monthly premium paid for health insurance, percent of premium paid by the company, reasons that influenced the decision to provide health insurance, whether a Health Maintenance Organization (HMO) insurance plan was offered, whether a deductible or co-payment was required for hospital inpatient services, and whether hospital room and board, physician office visits, maternity care, prescription drugs, inpatient mental health treatment, or substance abuse treatment were covered. These firms were also queried about recent changes in the number of health plan enrollees, deductibles, co-insurance rates, benefits offered, employer premium share, recent changes in health insurance carriers and reasons for changing, and recent increases in premiums and their effects on the firm's prices, profits, wages, and number of employees. Companies not offering health insurance were asked why they did not offer this benefit and were queried about factors that might influence them to offer a health plan. Individual-level data on employees include sex, age, marital status, length of employment, number of hours worked during the last week, salary or wage, health plan participation, amount of health premium paid by the employee, and whether the employee had health coverage from another source.

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Newly Licensed Registered Nurse Survey, 2011 (ICPSR 36814)

Released/updated on: 2020-01-30

Geographic coverage: United States

This is the fourth wave of a multi wave panel survey that studied newly licensed registered nurses who obtained their first license to practice between September 1, 2004 and August 31, 2005. It was conducted as part of the RN Work Project, a national study of new nurses funded by the Robert Wood Johnson Foundation. The survey interviewed the nurses about their jobs, turnover, intentions and attitudes--including intent, satisfaction, organizational commitment, and preferences about work.

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Newly Licensed Registered Nurse Survey, 2013 (ICPSR 36815)

Released/updated on: 2020-01-30

Geographic coverage: United States

This is the fifth wave of a multi wave panel survey that studied newly licensed registered nurses who obtained their first license to practice between September 1, 2004 and August 31, 2005. It was conducted as part of the RN Work Project, a national study of new nurses funded by the Robert Wood Johnson Foundation. The survey interviewed the nurses about their jobs, turnover, intentions and attitudes--including intent, satisfaction, organizational commitment, and preferences about work.

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Simple Crosstabs

Health Reform Monitoring Survey, United States, First Quarter 2013 (ICPSR 35624)

Released/updated on: 2019-05-16

Geographic coverage: United States

Time period: 2013-01-31--2013-02-11, 2013-02-26--2013-03-11

In January 2013, the Urban Institute launched the Health Reform Monitoring Survey (HRMS), a quarterly survey of the nonelderly population, to explore the value of cutting-edge, Internet-based survey methods to monitor the Affordable Care Act (ACA) before data from federal government surveys are available. Topics covered by the first round of the survey (first quarter 2013) include self-reported health status, type of and satisfaction with current health insurance coverage, access to and use of health care, and health care affordability. Additional information collected by the survey includes age, education, race, Hispanic origin, gender, income, household size, housing type, marital status, employment status, United States citizenship, smoking, internet access, home ownership, body mass index, sexual orientation, and whether the respondent reported an ambulatory care sensitive condition or a mental or behavioral condition.

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Newly Licensed Registered Nurse Survey, 2006 (ICPSR 36773)

Released/updated on: 2020-01-30

Geographic coverage: United States

This is the first wave of a multi wave panel survey that studied newly licensed registered nurses who obtained their first license to practice between September 1, 2004 and August 31, 2005. It was conducted as part of the RN Work Project, a national study of new nurses funded by the Robert Wood Johnson Foundation. The survey interviewed the nurses about their jobs, turnover, intentions and attitudes--including intent, satisfaction, organizational commitment, and preferences about work.

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Newly Licensed Registered Nurse Survey, 2015 (ICPSR 36816)

Released/updated on: 2020-01-30

Geographic coverage: United States

This is the sixth wave of a multi wave panel survey that studied newly licensed registered nurses who obtained their first license to practice between September 1, 2004 and August 31, 2005. It was conducted as part of the RN Work Project, a national study of new nurses funded by the Robert Wood Johnson Foundation. The survey interviewed the nurses about their jobs, turnover, intentions and attitudes--including intent, satisfaction, organizational commitment, and preferences about work.

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Medicare+Choice Survey, 2000: [United States] (ICPSR 3406)

Released/updated on: 2002-05-14

Geographic coverage: United States

This survey is one component of the Monitoring Medicare+Choice Project, a national study designed to provide information on health insurance decisions made by Medicare beneficiaries. Funded by the Robert Wood Johnson Foundation, the project examined how Medicare beneficiaries responded to the implementation of the Medicare+Choice provisions of the Balanced Budget Act of 1997. Among their multiple objectives, the Medicare+Choice provisions sought to expand substantially the types of coverage choices available to Medicare beneficiaries and to encourage beneficiaries to think more actively about these choices. The Medicare+Choice Survey interviewed a sample of Medicare beneficiaries about their basic knowledge of Medicare, current Medicare coverage options, sources of supplemental insurance coverage, satisfaction with current coverage, reasons for the most recent change in Medicare coverage or lack of change since September 15, 1999, sources of information used to make their coverage choices, and salience of the choice and its most relevant considerations. Additional information collected by the survey included the respondent's health and functional status, age, sex, marital status, race, Hispanic origin, education, reading ability, household income and the number of people supported by that income, and language spoken at home.

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National Survey of Primary Care Physicians and Nurse Practitioners, 2012 (ICPSR 36050)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 2011-11-23--2012-04-09

The focus of this survey was the role of nurse practitioners and physicians in primary care and the likely effects on the health care system of expanding the supply of nurse practitioners and their scope of practice. Topics of the survey include satisfaction with career, daily roles and responsibilities, perceived affects of increasing the supply of NPs, attitudes toward NP scope of practice, information on clinical practice services and revenue, and respondent demographics and income.

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National Survey of Alcohol, Drug, and Mental Health Problems [Healthcare for Communities], 1997-1998 (ICPSR 3025)

Released/updated on: 2006-03-30

Geographic coverage: United States

Time period: 1997-01-01--1998-01-01

This survey is a component of the Robert Wood Johnson Foundation's Health Tracking Initiative, a program designed to monitor changes within the health care system and their effects on people. Focusing on care and treatment for alcohol, drug, and mental health conditions, the survey reinterviewed respondents to the 1996-1997 CTS Household Survey (COMMUNITY TRACKING STUDY HOUSEHOLD SURVEY, 1996-1997, AND FOLLOWBACK SURVEY, 1997-1998: [UNITED STATES] [ICPSR 2524]). Topics covered by the questionnaire include (1) demographics, (2) health and daily activities, (3) mental health, (4) alcohol and illicit drug use, (5) use of medications, (6) health insurance coverage including coverage for mental health, (7) access, utilization, and quality of behavioral health care, (8) work, income, and wealth, and (9) life difficulties. Five imputed versions of the data are included in the collection for analysis with multiple imputation techniques.

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Community Tracking Study Household Survey, 2000-2001: [United States] (ICPSR 3764)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 2000-01-01--2001-01-01

This collection comprises the third round of the Community Tracking Study (CTS) Household Survey. The CTS, sponsored by the Robert Wood Johnson Foundation, is a national study designed to track changes in the health care system and the effects of those changes on people. Fifty-one metropolitan areas and nine nonmetropolitan areas were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the Household Survey (ICPSR 2524 and 3199), the third round was administered to households in the 60 CTS sites and to a supplemental national sample of households. Respondents provided information about household composition and demographic characteristics, health insurance coverage, use of health services, unmet health care needs, out-of-pocket expenses for health care, usual source of care, patient trust and satisfaction, last visit to a medical provider, health status and presence of chronic health conditions, risk behaviors and smoking, and employment, earnings, and income. A new set of sample design variables was added to the third round data for variance estimation by statistical software packages other than SUDAAN.

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Pathways to Adulthood: A Three-Generation Urban Study, 1960-1994: [Baltimore, Maryland] (ICPSR 2420)

Released/updated on: 2019-11-26

Geographic coverage: Baltimore, United States, Maryland

Time period: 1960-01-01--1994-01-01

This collection incorporates both prospective and retrospective data on three generations of families initially living in inner-city Baltimore, Maryland. The prospective data were selected from data collected as part of the Johns Hopkins Collaborative Perinatal Study (JHCPS), a survey of pregnant women seeking prenatal care and delivery at Johns Hopkins Hospital during 1960-1964. JHCPS studied these women (the first-generation mothers, abbreviated as G1) and the children born to them during 1960-1965 (the second-generation children, abbreviated as G2) until the children were 8 years old. The retrospective data come from a follow-up study, conducted in 1992-1994, of G1, G2, and the children born to G2 (the third-generation children, abbreviated as G3). Data from JHCPS on G1 include obstetrical and reproductive history at registration for prenatal care, sociological/family history variables at or around delivery of G2, observations of mother with child when G2 was 4 months old and 8 months old, and family history, demographic, and sociological variables when G2 was age 7. For G2, the data from JHCPS include delivery room observations at birth, pediatric examination data at age 4 months, developmental evaluation data at age 8 months, pediatric-neurological examination data at age 12 months, language, hearing, and speech evaluation summary data at age 36 months, psychological, behavior profile, physical growth, and other tests at age 48 months, psychological, motor, behavior, neurological, vision, physical, and other tests at age 7-1/2 years, and language, hearing, and speech evaluations, physical growth, interval medical history, and other tests at age 8 years. Retrospective data from the follow-up study on G1 include variables on education, employment, family composition, health and health care usage, housing conditions, income and income sources, marital status, partnerships and changes, neighborhood characteristics at registration to JHCPS and current, and reproductive history. For G2, data from the follow-up include information on aspirations, education, schooling, employment, family composition, health and health care usage, housing conditions, income and income sources, legal problems, living arrangements, marriage, partnership and changes, neighborhood characteristics at birth, at ages 11/12 and 16/17, and current, reproductive history, social relationships, smoking, and substance abuse. Data for the assessed third-generation children, i.e., G3s who were 7-8 years old during the follow-up period, include information on cognitive development, academic achievement and behavior, prenatal care, health, day care, and parental aspirations.

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Newly Licensed Registered Nurse Survey, 2007 (ICPSR 36812)

Released/updated on: 2020-01-30

Geographic coverage: United States

This is the second wave of a multi wave panel survey that studied newly licensed registered nurses who obtained their first license to practice between September 1, 2004 and August 31, 2005. It was conducted as part of the RN Work Project, a national study of new nurses funded by the Robert Wood Johnson Foundation. The survey interviewed the nurses about their jobs, turnover, intentions and attitudes--including intent, satisfaction, organizational commitment, and preferences about work.

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Newly Licensed Registered Nurse Survey, 2009 (ICPSR 36813)

Released/updated on: 2020-01-30

Geographic coverage: United States

This is the third wave of a multi wave panel survey that studied newly licensed registered nurses who obtained their first license to practice between September 1, 2004 and August 31, 2005. It was conducted as part of the RN Work Project, a national study of new nurses funded by the Robert Wood Johnson Foundation. The survey interviewed the nurses about their jobs, turnover, intentions and attitudes--including intent, satisfaction, organizational commitment, and preferences about work.

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Community Tracking Study Physician Survey, 2000-2001: [United States] (ICPSR 3820)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 2000-01-01--2001-01-01

This study comprises the third round of the physician survey component of the Community Tracking Study (CTS). Sponsored by the Robert Wood Johnson Foundation, the CTS is a large-scale investigation of changes in the health care system and their effects on people. Central to the design of the CTS is its community focus. Sixty sites (51 metropolitan areas and 9 nonmetropolitan areas) were randomly selected to form the core of the CTS and to be representative of the nation as a whole. As in the first two rounds of the physician survey, COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1996-1997: [UNITED STATES] (ICPSR 2597) and COMMUNITY TRACKING STUDY PHYSICIAN SURVEY, 1998-1999: [UNITED STATES] (ICPSR 3267), the third round was administered to physicians in the 60 CTS sites and to a supplemental national sample of physicians. The survey instrument collected information on physician supply and specialty distribution, practice arrangements and physician ownership of practices, physician time allocation, sources of practice revenue, level and determinants of physician compensation, provision of charity care, career satisfaction, physicians' perceptions of their ability to deliver care, effects of care management strategies, and various other aspects of physicians' practice of medicine. Part 3, the Site and County Crosswalk Data File, identifies the counties that constitute each CTS site. Part 4, Physician Survey Summary File, contains site-level estimates and standard errors for selected physician characteristics, e.g., the average age of physicians, the percentage of physicians who were either very or somewhat dissatisfied with their overall career in medicine, and the average percentage of patients with prescription coverage that included the use of a formulary.

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Hospitalized Older Persons Evaluation (HOPE) Study, 1991-1993: [California] (ICPSR 6560)

Released/updated on: 2006-01-12

Geographic coverage: United States, California

Time period: 1991-03-01--1993-05-31

The HOPE study was a multi-center randomized clinical trial mounted to determine the effects of hospital inpatient consultative comprehensive geriatric assessment (CGA) under typical practice conditions on selected patient health and health services utilization outcomes. The main outcome measures were functional status, health status, mortality, rehospitalization, and total use of health care services for hospital patients 65 years of age and older. Functional status was evaluated by questions about limitations in patients' activities of daily living due to health problems. Also included were items covering living arrangements (with whom and where), ethnicity, education, and marital status. Health status questions covered patients' perceptions of mental health and current physical health. The functional and health status of patients was measured prior to CGA treatment and randomization, again at 3 months post-randomization, and at 12 months post-randomization. Functional and health status data are included in Parts 3-8. Health services utilization data (Parts 9-15) cover patient use of medical services such as urgent care, emergency room, radiology, durable medical equipment, and medications (prescribed and over the counter). Mortality information (Part 17) includes date of lost contact or death, and data source of survival status. Hospitalization measures (Part 18) include date of admission and discharge, admittance source diagnoses and procedures, and inpatient/outpatient status.

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Research on Pathways to Desistance [Maricopa County, AZ and Philadelphia County, PA]: Official Arrest Records, 2000-2010 [Restricted] (ICPSR 34605)

Released/updated on: 2014-07-24

Geographic coverage: United States, Phoenix, Arizona, Philadelphia, Pennsylvania

Time period: 2000-01-01--2010-01-01

The Pathways to Desistance study was a multi-site study that followed 1,354 serious juvenile offenders from adolescence to young adulthood in two locales between the years 2000 and 2010. Enrolled into the study were adjudicated youths from the juvenile and adult court systems in Maricopa County (Phoenix), Arizona (N=654), and Philadelphia County, Pennsylvania (N=700).

The official arrests records of all 1,354 youth were obtained from multiple sources. For arrest/petitions under the age of 18, this information is based on petitions appearing in the juvenile and adult court records in each site. In Philadelphia, this information was gathered based on a hand review of juvenile and adult court documents; in Phoenix, the information is based on reports from two computerized court tracking systems (JOLTS--Juvenile On-Line Tracking System for juvenile court information, ICIS--Maricopa County Superior Court database for adult court information). For arrests/petitions over 18, FBI arrest records are the source of information. There is no self-reported information contained in this set of data.

Information from these different data sources is consolidated into the following categories:

Information regarding petitions with a date that falls prior to the baseline interview date ("prior petitions").
Information regarding the study index petition (also called the "initial referring petition"; this is the adjudication that prompted study enrollment). Information regarding the study index petition can be found by accessing the "type" variable associated with the prior petitions (specific variable name: Official Record Prior PetitionXX: Petition type). Depending on the investigator's needs, this petition can remain combined with the "priors" or be used as a stand-alone petition.
Information regarding arrests and court petitions with a date which falls after the baseline interview date in the Pathways study ("rearrests").

Curated

Partially restricted

Evaluation of the Partnership for Long-Term Care (PLTC) [California, Connecticut, Indiana, and New York]: Surveys of PLTC/non-PLTC Insurers, Purchasers/Nonpurchasers of PLTC Insurance, and Purchasers of non-PLTC Insurance, 1995-1996 (ICPSR 2466)

Released/updated on: 2024-02-14

Geographic coverage: Indiana, United States, Connecticut, California, New York (state)

Time period: 1995-01-01--1996-01-01

These surveys were conducted to evaluate the Partnership for Long-Term Care (PLTC), a project in which the Robert Wood Johnson Foundation awarded grants to four states -- California, Connecticut, Indiana, and New York -- to work with private insurers to create long-term care insurance policies that were more affordable and provided better protection against impoverishment than those generally available. PLTC policies combine private long-term care insurance with special Medicaid eligibility standards that protect assets of the insured once private insurance benefits are exhausted. Four parts constitute this collection. Parts 1 and 2 consist of data from a survey of PLTC insurers and of non-PLTC insurers, respectively. Both of these surveys gathered information on marketing methods, underwriting procedures, case management, sales, views on the PLTC, and reasons for participating or not participating in the PLTC. Part 3 comprises data from a survey of purchasers and nonpurchasers of PLTC policies, which included questions about health status, insurance coverage, opinions on long-term care insurance, financial planning for long-term care, income, assets, and demographic and social characteristics, such as sex, date of birth, education, race, Hispanic origin, marital status, household size, number of living children, and employment. Part 4 contains data from a survey of Californians who purchased non-PLTC long-term care insurance before and after the implementation of the PLTC in California. This survey covered the same topics as the survey of purchasers/nonpurchasers of PLTC insurance.

Curated

Partially restricted

Evaluating the Dental Pipeline Program: Recruiting Minorities and Promoting Community-Based Dental Education, 2003-2007 [United States] (ICPSR 25581)

Released/updated on: 2024-02-14

Geographic coverage: United States

Time period: 2002-01-01--2007-01-01

The Pipeline, Profession, and Practice: Community-Based Dental Education (Dental Pipeline) program was a national initiative created by the Robert Wood Johnson Foundation (RWJF) in 2001 to address the critical shortage of oral health care for underserved and disadvantaged populations in the United States. By 2003, RWJF selected 11 dental schools to receive Dental Pipeline funding for 5 years through a competitive application process, and The California Endowment (TCE) joined the program in July 2003, funding 4 additional dental schools in California. The initiative focused on recruitment and retention of underrepresented minority dental students, curriculum revisions to stress community-based dental education (CBDE), and increased extramural clinical rotations for students in the community, with the expectation that these changes in dental education would lead to improved access for underserved populations. The Dental Pipeline program sought not only to increase underrepresented minority recruitment but also to build cultural competence for all dental students so that they are better prepared to treat a diverse group of patients. Based in the Department of Health Services at the UCLA School of Public Health, the National Evaluation Team (NET) was chosen by the foundations to be the national evaluator of the Pipeline program. The NET employed a multidisciplinary team using qualitative and quantitative methods and multiple data sources to conduct a comprehensive 5-year evaluation. This ICPSR study contains data from five of the evaluation's data collection efforts: two faculty surveys, a survey of deans, curriculum checklists, clinical information system, and site-visit interviews.

Conducted at two time points during the Pipeline program implementation, the faculty surveys interviewed faculty members in the Dental Pipeline schools about their perceptions of extramural clinical rotations; competence of senior students; support for and effectiveness of recruitment programs intended to increase the number of underrepresented minority and low-income (URM/LI) dental students; impact of diversity on education experience; barriers to sustainability of the extramural programs, cultural competency dental education curricula, and URM/LI recruitment; and barriers for graduating seniors to practice in settings that provide care to underserved populations.

The survey of deans from Pipeline schools inquired about the importance of public policy issues related to dental education and expanding access to oral health care, level of activity and effectiveness of efforts to influence goals, and factors that facilitate or serve as barriers to influencing policy development.

The purpose of the curriculum checklists was to document the Pipeline schools' efforts to develop/revise their CBDE curricula and to characterize the key parameters of all their CBDE courses.

The clinical information system collected information about the Pipeline schools' predoctoral clinical rotations for each of the five academic years covered by the evaluation: total number of days in core community rotations, number of days in extramural rotations by type of extramural site (e.g., urban/rural, Federally Qualified Health Center, community health center, Veterans Administration hospital/clinic, Indian Health Service, and public/parochial school), and average distance of extramural facilities from school.

Multiple rounds of qualitative site visit interview data were collected from different stakeholder groups at the Pipeline schools: faculty, administrators, community representatives, first year students, and fourth year students. The site visit interviews, which were taped and transcribed, were conducted for several reasons: to describe Pipeline program components including baseline status, program structures, and implementation processes; to validate and clarify information gathered from other data sources; to collect information not available from other data sources; and to identify evidence-based best practices in the schools. Altogether, there are 522 discrete transcripts which ICPSR bundled in a single ZIP archive.