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Strong Heart Study (SHS)
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Sample details

The SHS is a study of cardiovascular disease and its risk factors among Native American (also called American Indian, First American, or Indigenous American) men and women in the United States of America. At baseline, the study initially included over 4,500 participants aged 45-74 years, recruited across 12 Native American tribal nations and communities, including the Gila River Indian Community (GRIC) and Salt River Indian Community(SRIC) in Arizona, the Apache, Caddo, Comanche, Delaware, Fort Sill Apache, Kiowa and Wichita tribal nations in Oklahoma, the Oglala Sioux, and Cheyenne River Sioux tribal nations in South Dakota and the Devil's Lake Sioux tribal nation in North Dakota. From 2001-2003, the study was expanded to include a family cohort to investigate the genetic contributions to cardiovascular disease and its risk factors (Strong Heart Family Study, SHFS). The SHFS included over 3,700 individuals aged at least 15 years from 94 extended families, including over 800 family members of the original SHS cohort.

Study design
Cohort

Number of participants at first data collection

4,549 (SHS participants)

3,776 (SHFS participants)

Age at first data collection

45 - 74 years (SHS participants)

≥ 15 years (SHFS participants)

Participant year of birth

Varied (SHS participants)

Varied (SHFS participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Families
First Nations Peoples
Indigenous peoples
Racial and ethnic minorities
Dataset details

Country

United States of America

Year of first data collection

1989

Primary Institutions

University of Oklahoma (OU)

Links

strongheartstudy.org/

nhlbi.nih.gov/science/strong-heart-study-shs

Funders

National Heart, Lung, and Blood Institute (NHLBI)

National Institutes of Health (NIH)

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Interview – unspecified
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – unspecified
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • Patients, service users, lived experience involvement
  • Community engagement
  • Participant or community advisory groups
  • Keywords

    Biological samples/biospecimens
    Cardiovascular health and disease
    Genetic factors
    Morbidity and mortality
    Risk factors
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