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Community Tracking Study (CTS)
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Sample details

The Community Tracking Study (CTS) is a comprehensive, longitudinal investigation into health system changes across the United States, involving approximately 60,000 individuals and around 12,000 physicians from 60 nationally representative communities. Initially, 48 of these communities were large metropolitan areas, with 12 selected for in-depth study through larger survey samples and site visits. The study includes a nationally representative cohort comprised of households, health plan leaders, and physicians, each providing detailed information on various aspects of health care. Participants for the Household Survey were recruited through random sampling, while thousands of physicians contributed data through the Physician Survey and interviews. Additionally, an Employer Health Insurance Survey was conducted exclusively during the first round of data collection (1996-1997). Since its inception, the study has continued to collect data at two-year intervals. In the fifth round of data collection (2007), the community-based design was replaced by a national-sample design, although site visits continued to focus on the 12 communities. Subsequent rounds are referred to as the Health Tracking Household Survey. The study has completed six rounds of site visits, with the latest occurring in 2010-2011.

Study design
Cohort

Number of participants at first data collection

60,446 (household participants)

12,385 (physician participants)

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
Of the population of the United States of America.

Sample features

Healthcare workers
Households and household members
Medical doctors
Dataset details

Country

United States of America

Year of first data collection

1996

Primary Institutions

Center for Studying Health System Change (HSC)

Links

hschange.org/CONTENT/80/index.html

pmc.ncbi.nlm.nih.gov/articles/PMC1089112/

Profile paper DOI

jstor.org/stable/29772621

Funders

Robert Wood Johnson Foundation

Ongoing?
No

Data types collected

qualitativeData
Quantitative data collection
  • Interview – face-to-face
  • Interview – phone
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • None
Features

Engagement

  • Community engagement
  • Keywords

    Community
    Health insurance
    Healthcare access and use
    Healthcare guidelines
    Healthcare workers
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