4.4 Article

The HealthStreet Cancer Survivor Cohort: a Community Registry for Cancer Research

Journal

JOURNAL OF CANCER SURVIVORSHIP
Volume -, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1007/s11764-022-01173-4

Keywords

Cancer survivors; Community outreach and engagement; Disparity; Rural; Research participation

Funding

  1. National Clinical and Translational Science Award [UL1 TR001427]
  2. National Cancer Institute [K07 CA201334]
  3. National Institutes of Health

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This report describes a cancer survivor cohort from a community engagement program and compares characteristics and willingness to participate in health research between the cancer survivors and non-cancer community members. The study found that cancer survivors from this program are diverse in terms of geography, race, and social determinants of health, and have a higher interest in participating in research.
Purpose This report describes a cancer survivor cohort from a community engagement program and compares characteristics and willingness to participate in health research between the cancer survivors and non-cancer community members. Methods Among 11,857 members enrolled in HealthStreet at the University of Florida (10/2011-03/2020), 991 cancer survivors were identified and 1:1 matched to control members without cancer on sex, age, and zip code. Demographics, body weight, height, social determinants of health, history of cancer, and willingness to participate in research were recorded by Community Health Workers as a part of the baseline Health Needs Assessment. Results Among the cancer survivors, 71.6% were female and 19.2% lived in rural areas with a mean age of 56.7 years in females and 60.8 years in males. At baseline, 44.7% received a cancer diagnosis within 5 years, while 15.8%, more than 20 years. Cancer survivors (vs. matched non-cancer controls) were less likely to be Black (31.1% vs. 63.6%) but more likely to be divorced, separated, or widowed (49.5% vs. 41.2%), be normal/underweight (34.0% vs. 25.6%) and have health insurance (80.0% vs. 68.6%; all p < 0.05). Cancer survivors versus matched controls reported higher rates of ever being in a health research study (32.4% vs. 24.9%) and interest in participating in studies ranging from minimal risk to greater-than-minimal risk. Conclusions Cancer survivors from this community engagement program agnostic to cancer types and treatment are diverse in geography, race, and social determinants of health and can be a valuable resource for observational, interventional, and biospecimen research in cancer survivorship.

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