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Showing 1 – 22 of 22 results.
Curated

Boston Rehabilitative Impairment Study of the Elderly (Boston RISE), 2009-2015 (ICPSR 37045)

Released/updated on: 2021-01-28
Geographic coverage: Massachusetts, Boston
Time period: 2009-01-01--2015-01-01
The Boston Rehabilitative Impairment Study of the Elderly (Boston RISE) was a prospective cohort study of older primary care patients, aged 65 years and older, who were at risk for declining mobility and disability at baseline. The study was designed to investigate which combinations of neuromuscular impairments are most responsible for mobility decline and disability over 2 years of follow up. Through additional funding, Boston RISE continued to collect follow up data on the Late Life Function and Disability Instrument (LLFDI) and mobility-related and healthcare utilization outcomes over the phone as part of a 2-year extension. Several ancillary measures were also collected throughout the course of the study.
Curated

CTDA 1003: Development of the Acute Stress Checklist for Children (ASC-Kids) in Children Age 8 to 17, United States, 2002-2004 (ICPSR 38902)

Released/updated on: 2024-01-24
Geographic coverage: United States
Time period: 2002-01-01--2004-01-01

Exposure to traumatic events is a common experience for children and adolescents. Accurate early assessment of acute stress responses can help predict risk for longer term sequelae and can guide secondary prevention to reduce the incidence and severity of post-traumatic stress disorder (PTSD) after trauma exposure.

The goal of this project was to develop a practical self-report measure of acute stress disorder (ASD) for children and adolescents, and to provide initial evidence as to its reliability and validity. The specific aims of the project were to:

  • Aim 1: Establish the content validity of a pilot Child ASD measure for ages 8 to 17, based on expert review and youth feedback.
  • Aim 2: In a sample of recently injured children (n=176), assess the psychometric properties of the measure: internal consistency, test-retest reliability, convergent and discriminant validity with other measures and other reporters.
  • Aim 3: Provide initial data regarding the predictive validity of the Child ASD measure in relation to later PTSD development in the same sample of children.
This collection includes data related to Aims 2 and 3.
Curated

CTDA 1004: Posttraumatic Stress in Youth Age 8 to 18 Seen in the Emergency Department for Violent Injury, United States, 1999-2000 (ICPSR 39170)

Released/updated on: 2024-07-22
Geographic coverage: United States
Time period: 1999-01-01--2000-12-31

Children and youth, aged 8 - 18 years, were invited to participate in this study after being treated in an emergency department (ED) for an injury resulting from interpersonal community violence. Each invited youth also had to have been living within specified postal codes (urban areas surrounding the hospital). Following the youth's baseline assessment (T1), participants completed between 0 and 4 follow-up assessments. The timing of each follow-up assessment was scheduled according to the relative time since the index (violent injury) event occurred. The average follow-up assessment was conducted at 27 days (T3), 75 days (T5), 199 days (T7), and 467 days (T10).

Curated

CTDA 1005: Posttraumatic Stress and Depression Risk Screening in Children Age 8 to 17 Seen in the Emergency Department for Unintentional Injury and Their Parents, United States, 2003 (ICPSR 39173)

Released/updated on: 2025-05-27
Geographic coverage: United States

After pediatric injury, posttraumatic stress and other emotional outcomes in children and their parents often go unrecognized and untreated. This is due in part to the challenges in identifying at-risk children and their parents in the emergency care setting. The aims of this study were to assess the extent to which nurses were able to implement a brief screener for posttraumatic stress symptoms risk within the course of normal care of injured patients, and to assess posttraumatic stress and depression symptoms in injured children (aged 8-17 years) and their parents after emergency department care, and the relationship of these symptoms to parent-reported overall recovery.

Curated

CTDA 1006: Validation of the Acute Stress Checklist for Children (ASC-Kids) in English & Spanish in Children Age 8 to 17, United States, 2007-2010 (ICPSR 39036)

Released/updated on: 2024-03-18
Geographic coverage: United States
Time period: 2007-01-01--2010-01-01
Validated Spanish-language measures of child traumatic stress are needed to assess Spanish-speaking children in the United States. This study built on the development of self-report checklist measures for acute stress disorder (ASD) in children, primarily the Acute Stress Checklist for Children (ASC-Kids), in English and Spanish. The prospective study assessed the reliability, validity, and factor structure of these child self-report measures by enrolling parallel samples of English- and Spanish-speaking children and adolescents (age 8-17 years) recruited in inpatient and outpatient settings associated with academic medical centers in the United States.
Curated

CTDA 1008: Posttraumatic Stress in Children Age 8 to 17 Hospitalized or Seen in the Emergency Department for Unintentional Injury, United States, 2005-2006 (ICPSR 39182)

Released/updated on: 2025-05-27
Geographic coverage: United States
Time period: 2005-01-01--2006-01-01

The objectives of the current study were to describe child post-traumatic stress (PTS), coping behavior, and parent coping assistance following a child's injury. The study enrolled children age 8 to 17 treated at the emergency department or admitted to the hospital for unintentional injury, and one parent per child. Children and parents completed measures of child PTS, coping, and coping assistance at 2 weeks post-injury and 3 months post-injury. The research team addressed these questions:

  1. What types of coping do children use following an injury?
  2. Is parent coping assistance related to child coping behavior?
  3. Are child coping strategies associated with PTS symptoms?
  4. Is early parent coping assistance related to later development of child PTS symptoms?

This study was originally conceived as a prospective randomized trial to evaluate the efficacy of secondary prevention messages conveyed in printed informational materials (handouts and workbooks) for children and parents after pediatric injury. Children and their parents received 1 of 5 randomly assigned workbook sections (each addressing a different key theme). No differences were observed between groups for parent/child knowledge and beliefs about PTS and adaptive coping, nor in child PTS symptoms. Thus, data from all groups have been combined for analyses of prospective PTS outcomes and coping processes.

Curated

CTDA 1009: Posttraumatic Stress and Depression in Adolescents Age 12 to 17 Seen in the Emergency Department for Violent Injury, United States, 2001-2003 (ICPSR 39195)

Released/updated on: 2025-03-04
Geographic coverage: United States
Time period: 2001-01-01--2003-01-01

Because the emergency department (ED) is often the only point of contact with the health care system for violently injured adolescents, it provides a unique opportunity to assess children following a violent injury. In violently injured teens, depressive and acute posttraumatic stress symptoms may help predict future behavioral risk factors and reinjury. The objective of this study was to examine whether emergency department (ED) assessments of depressive and posttraumatic stress symptoms after an episode of interpersonal violence are associated with future risk behaviors, re-injury and posttraumatic stress symptoms in adolescents.

Injured adolescents (age 12-17 years) were assessed for posttraumatic stress and depression symptoms and self-reported risk behaviors either during or soon after (within 2 weeks) an ED visit and completed a telephone follow-up assessment between 6 and 18 months later, during which they were assessed again for self-reported risk behaviors, posttraumatic stress symptoms and re-injury.

Curated

CTDA 1010: Posttraumatic Stress in Children Age 6 to 16 Hospitalized for Accident-Related Injury and Their Parents, Australia, 2000-2004 (ICPSR 39198)

Released/updated on: 2025-05-27
Geographic coverage: Australia
Time period: 2000-01-01--2004-01-01

Trajectory modeling can identify patterns of posttraumatic stress symptoms in children and parents. This study aimed to describe trajectories of child and parent posttraumatic stress symptoms across 2 years post-injury, and to examine potential risk factors predicting problematic trajectories. The study enrolled children age 7 to 16 admitted to general or intensive care units for treatment of accidental injury, and one parent/caregiver per child. Within 2 weeks of injury, and at 4-6 weeks, 6 months, and (a subset) at 2 years post-injury, children and parents were assessed for posttraumatic stress symptoms. Parents also completed measures of parenting behavior and pre-injury child mental health.

Curated

CTDA 1013: Posttraumatic Stress in Children Age 6 to 15 Hospitalized for Traumatic Brain Injuries, Australia, 2004-2008 (ICPSR 39602)

Released/updated on: 2026-05-19
Geographic coverage: Australia
Time period: 2004-01-01--2008-01-01

This study prospectively assessed psychological and cognitive sequelae of traumatic brain injury (TBI) in children. Multiple factors may influence children's functioning following head injury including injury severity, pre-injury child factors, and family factors. Overall study aims were to describe the relationships between these factors and children's recovery in the eighteen months following their injury, to examine the relationship between children's cognitive impairments post injury and psychological distress related to the injury event, and to examine the role of PTSD in children's recovery from TBI.

The study enrolled children age 6 to 15 admitted to hospital after an accident resulting in mild to severe TBI, and one parent per child. Children and parents completed research assessments within 2 months of the accident, and at 3, 6, 12, and 18 months post-accident. Child health and behavior, health-related quality of life, parenting, and parent posttraumatic stress were assessed at all time points, and child posttraumatic stress symptoms were assessed at 3, 6, 12, and 18 months.

Curated

CTDA 1022: Posttraumatic Stress in Children Age 7 to 17 Seen in Hospital for Acute Injury, Australia, 2004-2006 (ICPSR 39196)

Released/updated on: 2024-09-18
Geographic coverage: Australia
Time period: 2004-01-01--2007-01-01

The broad aims of this overall project were to examine predictors of children's adjustment, mainly post-traumatic stress disorder (PTSD), after a single-incident injury. The overarching hypothesis was that a combination of physiological/biological, cognitive, and parental anxiety factors would predict children's later adjustment. The dataset in this collection comes from the combination of two broad projects that recruited from the same hospitals, with the first (smaller) project being built upon by the second project (which contained additional measures and an additional follow-up).

Children and adolescents aged 7 to 17 and their families (n=135) were recruited for the study after presentation to either of two major metropolitan Australian hospitals following a single-incident injury. Children's heart rate was recorded at hospital triage. Children and parents completed risk screening measures within 4 weeks of injury. Measures for cognitive appraisals, social support, traumatic stress, depression, and anxiety symptoms were assessed at 3 months and 6 months post-injury.

Curated

CTDA 1032: Posttraumatic Stress in Children Age 7 to 15 Hospitalized for Burn or Traffic Injury and Their Parents, Switzerland, 2016-2018 (ICPSR 39197)

Released/updated on: 2024-09-16
Geographic coverage: Switzerland
Time period: 2016-01-01--2018-01-01

This study enrolled children ages 7 to 15 who received medical care at the hospital after an acute traffic accident or burn injury, and up to two parents/caregivers per child. Within 1 month of injury, and at 3 months, and 6 months post-injury, children and parents were assessed for posttraumatic stress symptoms (PTSS) and depression. Parents also completed measures of their own anxiety symptoms and of child behavior and health-related quality of life. The study aimed to achieve a better understanding of dysfunctional trauma-related cognitions considering child and environmental factors in a cross-sectional and a longitudinal design.

Curated

CTDA 1036: Posttraumatic Stress, Appraisals, and Coping in Children Age 8 to 13 Hospitalized for Injury and Their Parents, United States, 2012-2015 (ICPSR 39433)

Released/updated on: 2025-07-23
Geographic coverage: United States
Time period: 2012-01-01--2015-01-01

Millions of children suffer unintentional injuries annually. While the majority display transient psychological distress, a significant minority develop significant, persistent symptoms of posttraumatic stress disorder (PTSD) that are associated with poorer general health outcomes and impaired quality of life. Understanding variables that contribute to the development of PTSD is an essential step in identifying children at increased risk for PTSD and improving secondary prevention to reduce the incidence of PTSD in children following medical events.

The objective of this study was to examine the interplay of biological, psychological (cognitive appraisals, coping), and environmental (parent influence) factors during the peri-trauma time period as these relate to the development of child PTSD symptoms over time.

Children age 8-13 with a recent injury (within the past 2 weeks) and one parent / caregiver per child were enrolled during an inpatient hospitalization. At the time of enrollment, and again 6 weeks and 12 weeks post-injury, children and parents completed measures of cognitive appraisals, coping, coping assistance, and PTSD symptoms. A brief parent-child interaction task was completed at the time of the baseline assessment - data from this task-based assessment are not included in this dataset.

Curated

Health Behavior in School-Aged Children, 2001-2002 [United States] (ICPSR 4372)

Released/updated on: 2008-07-24
Geographic coverage: United States
Time period: 2001-01-01--2002-01-01
Since 1982, the World Health Organization (WHO) Regional Office for Europe has sponsored a cross-national, school-based study of health-related attitudes and behaviors of young people. These studies, generally known as Health Behavior in School-Aged Children (HBSC), are based on independent national surveys of school-aged children in as many as 30 participating countries. The HBSC studies were conducted every four years since the 1985-1986 school year. The data available here are from the results of the United States survey conducted during the 2001-2002 school year. The study results can be used as stand-alone data, or to compare with the other countries involved in the international HBSC. The HBSC study has two main objectives. The first objective is to monitor health-risk behaviors and attitudes in youth over time to provide background data and to identify targets for health promotion initiatives. The second objective is to provide researchers with relevant information in order to understand and explain the development of health attitudes and behaviors through early adolescence. The study contains variables dealing with many types of drugs such as tobacco, alcohol, marijuana, inhalants, and any other substances. The study examines the first time these substances were used and the frequency of their use. Other topics include questions about the person's health and other health behaviors. Some of these topics include eating habits, body image, health problems, family make-up, personal injuries, bullying, fighting, and bringing weapons to school. A school administrator and the lead health education teacher also completed individual surveys concerning school programs and policies that affect students' health and the content of various health courses.
Curated

National Health Interview Survey, 2007 (ICPSR 27201)

Released/updated on: 2010-08-26
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Implementation of a redesigned NHIS, consisting of a basic module, a periodic module, and a topical module, began in 1997 (see NATIONAL HEALTH INTERVIEW SURVEY, 1997 [ICPSR 2954]). The 2007 NHIS contains the Household, Family, Person, Sample Adult, and Sample Child files from the basic module. Each record in Part 1, Household Level, contains data on type of living quarters, number of families in the household responding and not responding, and the month and year of the interview for each sampling unit. Part 2, Family Level, is made up of reconstructed variables from the person-level data of the basic module and includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, and employment status, along with industry and occupation. As part of the basic module, Part 3, Person Level, provides information on all family members with respect to health status, limitation of daily activities, cognitive impairment, and health conditions. Also included are data on years at current residence, region variables, height, weight, bed days, doctor visits, hospital stays, and health care access and utilization. A randomly-selected adult in each family was interviewed for Part 4, Sample Adult, regarding respiratory conditions, use of nasal spray, renal conditions, AIDS, joint symptoms, health status, limitation of daily activities, and behaviors such as smoking, alcohol consumption, and physical activity in addition to questions regarding stroke, diabetes, arthritis, and weight control. Part 5, Sample Child, provides information from an adult in the household on medical conditions of one child in the household, such as respiratory problems, seizures, allergies, and use of special equipment like hearing aids, braces, or wheelchairs. Also included are variables regarding child behavior, the use of mental health services, and Attention Deficit Hyperactivity Disorder (ADHD), as well as responses to the SDQ, the Strengths and Difficulties questionnaire on child mental health. The 2007 data contain the Child Conditions - Limitation of Activity and Health Status (CHS), Child Health Care Access and Utilization (CAU), Child Mental Health Brief (CMB), Child Mental Health Services (CMS) and Child Influenza Immunization (CFI) sections. Part 6, Injury/Poison Episode, is an episode-based file that contains information about the external cause and nature of the injury or poisoning episode and what the person was doing at the time of the injury or poisoning episode, in addition to the date and place of occurrence. Part 7, Injury/Poison Episode Verbatim, contains edited narrative text descriptions of the injury or poisoning, provided by the respondent. Part 8, Adult Complementary and Alternative Medicine, and Part 9, Child Complementary and Alternative Medicine, provide information regarding the use of 17 nonconventional health care practices, including acupuncture, movement therapies, and relaxation techniques, for sample adults and sample children, respectively. Supplemental Sample Child, Part 10, and Supplemental Sample Child Alternative Medicine, Part 11, are supplemental files for the 2007 data release. These files provide dummy records to fill in the missing information for Part 5, Sample Child, and Part 9, Child Complementary and Alternative Medicine. Part 12, Paradata, does not contain health related information, but rather data which are related to the interview process, including measures of time, contact-ability, and cooperation. RAT_CAT3 Update, Part 13, corrects an error in the 2007 Family Level variable RAT_CAT3.
Curated

National Health Interview Survey, 2008 (ICPSR 27341)

Released/updated on: 2010-08-26
Geographic coverage: United States
The purpose of the National Health Interview Survey (NHIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Implementation of a redesigned NHIS, consisting of a basic module, a periodic module, and a topical module, began in 1997 (see NATIONAL HEALTH INTERVIEW SURVEY, 1997 [ICPSR 2954]). The 2008 NHIS contains the Household, Family, Person, Sample Adult, and Sample Child files from the basic module. Each record in Part 1, Household Level, contains data on type of living quarters, number of families in the household responding and not responding, and the month and year of the interview for each sampling unit. Part 2, Family Level, is made up of reconstructed variables from the person-level data of the basic module and includes information on sex, age, race, marital status, Hispanic origin, education, veteran status, family income, family size, major activities, health status, activity limits, and employment status, along with industry and occupation. As part of the basic module, Part 3, Person Level, provides information on all family members with respect to health status, limitation of daily activities, cognitive impairment, and health conditions. Also included are data on years at current residence, region variables, height, weight, bed days, doctor visits, hospital stays, and health care access and utilization. A randomly-selected adult in each family was interviewed for Part 4, Sample Adult, regarding respiratory conditions, renal conditions, AIDS, joint symptoms, health status, limitation of daily activities, and behaviors such as smoking, alcohol consumption, and physical activity. Additionally, questions regarding oral health, asthma, balance, cancer screening, heart disease, HPV, immunization, and vision were fielded. Part 5, Sample Child, provides information from an adult in the household on medical conditions of one child in the household, such as respiratory problems, seizures, allergies, and use of special equipment like hearing aids, braces, or wheelchairs. Also included are variables regarding child behavior, Attention Deficit Hyperactivity Disorder (ADHD), oral health, asthma, indoor tanning, HPV, immunization, mental health, and vision. Part 6, Injury/Poison Episode, is an episode-based file that contains information about the external cause and nature of the injury or poisoning episode and what the person was doing at the time of the injury or poisoning episode, in addition to the date and place of occurrence. Part 7, Injury/Poison Episode Verbatim, contains edited narrative text descriptions of the injury or poisoning, provided by the respondent. Part 8, Paradata, does not contain health related information, but rather data which are related to the interview process, including measures of time, contact-ability, and cooperation.
Curated

National Hospital Ambulatory Medical Care Survey, 2005 (ICPSR 28261)

Released/updated on: 2010-06-08
Geographic coverage: United States
The National Hospital Ambulatory Medical Care Survey (NHAMCS) provides data from samples of patient records selected from emergency departments (EDs) and outpatient departments (OPDs) of a national sample of hospitals. The resulting national estimates describe the use of hospital ambulatory medical care services in the United States. For the 2005 survey, data were collected from 205 OPDs and 417 EDs. Among the variables included are age, race, and sex of the patient, reason for the visit, physician's diagnoses, cause of injury, surgical procedures (OPDs only), medication therapy, and expected source of payment. For 2005, additional updates and revisions have been made to both the emergency department and outpatient department data, including modifications to preexisting variables and the inclusion of new variables pertaining but not limited to patient pregnancy, height, and weight.
Curated

National Hospital Ambulatory Medical Care Survey, 2007 (ICPSR 28442)

Released/updated on: 2010-06-24
Geographic coverage: United States
The National Hospital Ambulatory Medical Care Survey (NHAMCS) provides data from samples of patient records selected from emergency departments (EDs) and outpatient departments (OPDs) of a national sample of hospitals. The resulting national estimates describe the use of hospital ambulatory medical care services in the United States. For the 2007 survey, data were collected from 202 OPDs and 432 EDs. Among the variables included are age, race, and sex of the patient, reason for the visit, physician's diagnoses, cause of injury, surgical procedures (OPDs only), medication therapy, and expected source of payment. For 2007, additional updates and revisions have been made to both the emergency department and outpatient department data, including modifications to pre-existing variables pertaining but not limited to electronic medical records.
Curated

National Hospital Ambulatory Medical Care Survey, 2008 (ICPSR 29922)

Released/updated on: 2011-01-18
Geographic coverage: United States
The National Hospital Ambulatory Medical Care Surveys (NHAMCS) provide data from samples of patient records selected from emergency departments (EDs) and outpatient departments (OPDs) of a national sample of hospitals. The resulting national estimates describe the use of hospital ambulatory medical care services in the United States. For the 2008 survey, data were colected from 209 OPDs and 431 EDs. Among the variables included are age, race, and sex of the patient, reason for the visit physician's diagnoses, cause of injury, surgical procedures (OPD's only), medication therapy, and expected source of payment. The 2008 survey remains unchanged from the previous year.
Curated

National Mortality Followback Survey, 1993 (ICPSR 2900)

Released/updated on: 2005-02-21
Geographic coverage: United States
The National Mortality Followback Survey (NMFS) Program, begun in the 1960s by the National Center for Health Statistics (NCHS), uses a sample of United States residents who die in a given year, supplementing information derived from the death certificate with information from the next of kin or another person familiar with the decedent's life history. This information, sometimes enhanced by administrative records, is collected in order to study the etiology of disease, demographic trends in mortality, and other health issues. The 1993 National Mortality Followback Survey (NMFS) sampled individuals aged 15 years and over who died in 1993. Forty-nine of the 50 state vital registration areas, as well as the independent vital registration areas of the District of Columbia and New York City, granted approval to sample their death certificates. (South Dakota declined to participate due to a state law restricting the use of death certificate information.) A sample of 22,957 death certificates from 1993 was then drawn. To obtain reliable numbers for important population subgroups, such as persons under age 35, women, and the Black population, death certificates from those subgroups were oversampled. The 1993 NMFS survey focused on five subject areas: (1) socioeconomic differentials in mortality, (2) associations between risk factors and cause of death (use of tobacco, alcohol, drugs, firearms, motor vehicles), (3) disability (medical condition and cognitive functioning during the last year of life), (4) access and utilization of health care facilities during the last year of life (number of doctor visits, days bedridden, nursing home experiences, use of assistive medical devices, availability of health insurance), and (5) reliability of certain items reported on the death certificate. Demographic variables include age, gender, race, marital status, birthplace, education, occupation and industry, and income and assets. The 1993 NMFS survey differed from the previous mortality followback surveys in several ways: First, it emphasized deaths due to homicide, suicide, and unintentional injury. Second, the subject areas were considerably broader (many previously-surveyed subject areas, however, are included for trend analysis). This survey was also the first to acquire national-level information from medical examiners and coroners. Finally, the complexity of the questionnaire necessitated telephone or in-person interviews. The 1993 NMFS was designed in collaboration with other agencies of the Public Health Service, Department of Health and Human Services, and the National Highway Traffic Safety Administration.
Curated

Norwegian Life History Study, 1971 (ICPSR 8545)

Released/updated on: 2006-01-12
Geographic coverage: Norway, Global
Time period: 1921-01-01--1971-01-01
This data collection represents interviews with birth cohorts of Norwegian males born in 1921, 1931, and 1941 who were 50, 40, and 30 years of age at the time the interviews were conducted (November 1971 - March 1972). The objective of the study was to investigate historical life changes in the life cycle experiences of Norwegian men. The respondents were asked about the families into which they were born, their childhoods, and their lives from the age of fourteen until the time of the interview. The major areas covered in the interviews include: place of residence, education, work history, income, household status and composition, marital status and family composition, illness and injuries, and receipt of benefits.
Curated

The Survey of Health, Ageing and Retirement in Europe (SHARE) -- Israel, 2005-2006 (ICPSR 22160)

Released/updated on: 2008-11-21
Geographic coverage: Israel, Global
Time period: 2005-01-01--2006-01-01

The Survey of Health, Ageing and Retirement in Europe (SHARE) is a multidisciplinary and cross-national database of micro data on health, socio-economic status and social and family networks of individuals aged 50 or over which was designed after the role models of the United States Health and Retirement Study (HRS) and the English Longitudinal Study of Ageing (ELSA).

SHARE-Israel was added to the collection during 2005 and 2006 and required a complex adaptation of the SHARE survey instruments for implementation in Israel. In order to access the three major population groups that make up Israeli society, veteran Jewish-Israelis, Arab-Israelis and new immigrants from the former Soviet Union after 1989, it was necessary to translate the CAPI questionnaire and the drop off questionnaire into Hebrew, Arabic and Russian.

Data collected include health variables (e.g., self-reported health, physical functioning, cognitive functioning, health behavior, use of health care facilities), psychological variables (e.g., psychological health, well-being, life satisfaction), economic variables such as (current work activity, job characteristics, opportunities to work past retirement age, sources and composition of current income, wealth and consumption, housing, education), and social support variables (e.g., assistance within families, transfers of income and assets, social networks, volunteer activities).

Two physical performance measures were also employed. The first was grip strength, the respondent's maximum handgrip strength measured by means of a dynamometer. The second physical performance measure was walking speed, which was asked only of persons aged 75 and older. This physical measurement involved asking the respondent to walk a certain distance and measuring the time it took for the respondent to complete the task.

Unique to SHARE-Israel were questions in the drop-off questionnaire regarding trauma. Respondents were asked about difficult life events that they had experienced and the degree to which they were affected by them. The events were drawn from the following areas (1) having personally suffered injury in war, in a terrorist attack, a grave illness or accident, (2) having witnessed injury or death in war, in a terrorist attack, and/or in an accident or crime, (3) having been a victim of crime, abuse, sexual harassment and/or severe economic adversity, (4) having had a close person injured or lost due to war, a terrorist attack, accident or grave illness, (5) loss of spouse and/or offspring, and (6) having provided or received long term care due to functional disability. A separate inventory chronicled respondents' exposure to the Holocaust.

Also included in the drop-off questionnaire were questions regarding pension reform: which addressed respondents' awareness of the legislated delay in the age of eligibility for retirement pension in Israel, (for men, age 67 and for women, age 64). It also inquired about implications of the change in pension age, information regarding personal plans for employment or retirement in light of the change, and sources of income that would be used to bridge the period between retirement and receipt of pension, if early retirement was contemplated. Full details regarding SHARE can be located at the SHARE Web site.

Curated
Simple Crosstabs

Swedish Adoption/Twin Study on Aging (SATSA), 1984, 1987, 1990, 1993, 2004, 2007, and 2010 (ICPSR 3843)

Released/updated on: 2015-05-13
Geographic coverage: Sweden, Global
Time period: 1984-01-01--2010-01-01
The Swedish Adoption/Twin Study on Aging (SATSA) was designed to study the origins of individual differences in aging and the environmental and genetic factors that are involved. SATSA began in 1984, and six additional waves were conducted in 1987, 1990, 1993, 2004, 2007, and 2010. The questionnaire was initially sent to all twins from the Swedish Twin Registry who were separated at an early age and raised apart; the survey was also administered to a control sample of twins who were raised together. The respondents were surveyed on items that included health status, how they were raised, work environment, alcohol consumption, and dietary and smoking habits, as well as questions about personality and attitudes; this information comprised the first component. The second component was collected from a subsample composed of 150 pairs of twins raised apart and 150 pairs of twins raised together. This subsample participated in seven waves of in-person testing, which included a health examination, structured interviews, and tests on functional capacity, cognitive abilities, and memory. The data are represented according to questionnaire and time number, and correspond to each wave/year: Questionnaire 1 and In-Person Testing Time 1 were in 1984; Questionnaire 2 and In-Person Testing Time 2 were in 1987; Questionnaire 3 and In-Person Testing Time 3 were in 1990; Questionnaire 4 and In-Person Testing Time 4 were in 1993; Questionnaire 5 was in 2003; In-Person Testing Time 5 was in 2004; Questionnaire 6 and In-Person Testing Time 6 were in 2007; In-Person Testing Time 7 was in 2010. The Administrative and Cognitive datasets include data from all years/waves. The Smell Survey dataset only includes data from 1990. No years were specified for the Contact measures and Separation measures datasets. Demographic and background information includes age, sex, education, family history, household composition and employment.
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