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Evaluating an Evidence-Based Family History Screening Program Adapted to Increase Reach and Uptake of Screening for BRCA-Associated Cancers in Rural Public Health Clinics

Emory University · with National Cancer Institute (NCI) · NCT06760507

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 25+ · Women only
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
3209
US sites recruiting
1
Study start
February 1, 2025
Record last updated
May 26, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This clinical trial adapts and evaluates the effectiveness of a family history screening program (GA CORE) for increasing uptake of genetic screening for BRCA-associated cancers in women who have received care in rural public health clinics in Southwest Georgia. Brief and low-cost family history-based screening assessments to identify families at high risk for BRCA-associated cancers have been endorsed by national guidelines and public health organizations. Georgia is among the few states to have implemented statewide family history screening for BRCA-associated cancers. Despite its potential, current clinic-based approaches that identify at-risk women are not sustainable and show limited reach. Additionally, uptake of follow-up cancer screening is sub-optimal and solely focuses on women screened as high genetic risk. This trial will adapt the existing family history screening program and then evaluate it's effectiveness for increasing the number and diversity of women who receive a history assessment and subsequent access to risk-based services such as genetic counseling and testing.

Being studied: Adapted Family History Screening Program

Conditions: Breast Cancer; Ovarian Cancer

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • AIM 1 STAKEHOLDER ADVISORY COMMITTEE: 10 stakeholders representing three constituencies: state cancer control leaders (n=2), participating public health district champions (n=4) (i.e., administrative directors, nurses, clinic staff) and patients (n=4) (i.e., women, age 25 and older who receive their care in the Southwest district)
  • AIM 1 DISCUSSION FORUM: 25 years or older
  • AIM 1 DISCUSSION FORUM: Women
  • AIM 1 DISCUSSION FORUM: English-speaker
  • AIM 1 DISCUSSION FORUM: Have completed family history screening during the first 3 months of the project at one of 14 public health clinics in Southwest district
  • AIM 1 ORGANIZATIONAL STAKEHOLDER INTERVIEW: Organizational stakeholders (i.e., medical directors, nurses, and clinic staff) at the 14 clinic sites in Southwest district
  • AIM 2: Women
  • AIM 2: Ages 25 and older
  • AIM 2: Who can read English
  • AIM 2: Have ever been seen in Women's Health Section through one of participating public health clinics in Southwest district
  • AIM 3 POST-INTERVENTION INTERVIEW: Participants from aim 2, regardless of whether they completed the recommended genetic services or not (e.g. complete telegenetic session or genetic testing)
  • AIM 3 WORKSHOP DISCUSSION: Medical and administrative directors, nurses, and clinic staff from the six participating clinic sites

Recruiting US locations

  • Emory University Hospital/Winship Cancer Institute

    Atlanta, GA 30322

    Site contact: Yue Guan · 404-712-1671 · yue.guan@emory.edu

Study contacts (from the official record)

  • Yue Guan, PhD · 404-712-1671 · yue.guan@emory.edu
All healthy volunteers studies in Georgia →
Evaluating an Evidence-Based Family History Screening Program… (NCT06760507) | Bored Studies