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Dataset: Health and Retirement Study (HRS)

Basic Information
Dataset full name: Health and Retirement Study
Dataset acronym HRS
Summary The Health and Retirement Study (HRS) is a nationally representative longitudinal panel survey conducted biennially. The study follows a cohort(s) of adults ages 50 years or older in the United States. The purpose of the HRS is to understand health shifts in older adults and demographic changes in labor force participation at the end of their service. It provides detailed information on demographic characteristics, income, work, assets, housing, pension plans, health insurance, disability, physical health and functioning, cognitive functioning, and health care expenditures. The original study began in 1992 and reinterviews the respondent and their spouse or partner every two years using an in-depth questionnaire. A new cohort is added to the sample every six years. In 1998, the original HRS was merged with Asset and Health Dynamics Among the Oldest-Old (AHEAD, born before 1923). In 1998, the HRS also included a Children of the Depression cohort (CODA, born 1923-1930) and a War Baby cohort (WB, born 1942-1947). In 2004, an Early Baby Boomer cohort (EBB, born 1948-1953) was added, a Mid Baby Boomers cohort (MBB, born 1954-1959) was added in 2010, and a Late Baby Boomers cohort (LBB, born 1960-1965) was added in 2016. Off-year questionnaires are also submitted to a subset of HRS respondents. These include: the Consumption and Activities Mail Survey (originating in 2001), the Disability Vignette Survey (2007), the Health Care and Nutrition Study (2013), the Human Capital and Educational Expenses Mail Survey (2001), the Life History Mail Survey (2015), the Internet Survey (originating in 2003), and the Veterans Mail Survey (2013).
Key Terms Aging, Longitudinal, Health, Income, Retirement, Disability, Housing, Pension, Family characteristics
Study Design Longitudinal
Data Type(s) Survey
Sponsoring Agency/Entity National Institutes of Health (NIH): National Institute on Aging (NIA) University of Michigan's Institute for Social Research
Health conditions/Disability measures
Health condition(s) Alzheimer’s/dementia, Arthritis, Body mass index (BMI)/obesity, Cancer, Cardiovascular conditions, Chronic pain, Depression, Diabetes, Eye diseases, Orthopedic conditions, Pulmonary disorders, Stroke
Disability Measures Ambulatory disability, Cognitive disability, Communication impairment, Functional limitations (ADLs and/or IADLs), Hearing disability, Independent living disability, Mental health disability, Physical disability, Self-care disability, Special equipment use/assistive technology, Visual Disability, Work limitation
Measures/outcomes of interest
Topics Income, Education, Internet use, Housing, Employment, Employer accommodations, Assets, Pension plans, Health insurance, Health care expenditures, Assistive Technology use
Sample
Sample Population Nationally representative sample of adults over the age of 50
Sample Size/Notes
Unit of Observation Individual
Geographic Coverage Initial (Wave 1) number of respondents in sample by cohort:
12,652 - HRS: Original R born 1931-1941
8,222 - AHEAD: Original R born in 1923 or earlier
2,320 - CODA (Children of Depression): Original R born 1924-1930
2,529 - WB (War Baby): Original R born 1942-1947
3,330 - EBB (Early Baby Boomers): Original R born 1948-1953
Sample size unavailable (as of publication) - MBB (Mid Baby Boomers): Original R born 1954-1959
Geographic specificity United States
Data Collection
Data Collection Mode National
Years Collected Primarily personal interview and phone surveys. Restricted data linkages available to the Employer Pension Study, National Death Index, Social Security Administration, and Medicare files.
Data Collection Frequency 1992-ongoing
Strengths and limitations
Strengths Biennial
Limitations Nationally-representative, multi-stage area probability sample. Excellent re-interview response rates of 90% or higher. Wide range of questions asked including: functional status, disability, economic factors, retirement, health services utilization, social security disability benefits, veterans’ benefits and workers’ compensation. The majority (80%) of HRS participants allow Medicare record based disease history data to be linked to their HRS data. **NOTE Medicare data access requires a Data Use Agreement (DUA) from the Centers for Medicare & Medicaid Services (CMS)**
Restricted data linkages include: biometric and biological information to the online genetics database of the National Institutes of Health (20,000 participants) , National Death Index, Social Security benefit and Medicare files.
Data details
Primary Website Information on chronic disease and health-care utilization are based on self-reports. Proxy responses used in about 20% of the 2008 core interviews for the oldest cohort (born 1890-1923) . Some question wording has been altered over time making some comparisons problematic. Questionnaire skip patterns and survey wave design can be difficult to follow.
Data Access https://hrs.isr.umich.edu/about
Data Access Requirements Data use agreement, No cost
Summary Tables/reports Access: http://hrsonline.isr.umich.edu/index.php?p=reg
Data products: https:// https://hrs.isr.umich.edu/data-products/
Dataset components (where applicable) The Health and Retirement Survey: Aging in the 21st Century. Challenges and Opportunities for Americans (2017, January).


http://hrsonline.isr.umich.edu/sitedocs/databook/inc/pdf/HRS-Aging-in-the-21St-Century.pdf
Selected papers
Technical Biennial Datasets Longitudinal Datasets Off-Year Studies Restricted data files
Other Papers https://hrs.isr.umich.edu/documentation/



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