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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04248257
Other study ID # STUDY00001007
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 15, 2020
Est. completion date December 2025

Study information

Verified date April 2023
Source Georgetown University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial will recruit young adult female relatives (YARs) of male or female carriers of BRCA1/2. YARs who consent to participate will be randomized to either a 3-session peer coach-led telephone counseling intervention or usual care navigation to peer support interventions provided by community organizations that support the hereditary cancer community. Study aims are to 1) Assess intervention effects on distress and decision making outcomes, including uptake of counseling for untested YARs, 2) Identify YARs most likely to engage with and benefit from the intervention, 3) Understand intervention mechanisms. Participants will complete interviews at baseline, 1, 6, and 12 months.


Recruitment information / eligibility

Status Recruiting
Enrollment 560
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - There are two targets for recruitment with different eligibility criteria. Index carriers: - Men or women aged 18 or older with BRCA mutations with or without 2nd-tier multiplex panel genetic testing. Index carriers will have received testing. YARs: - Female 1st-, 2nd- or 3rd-degree biological relatives of index carriers aged 21-30. Exclusion Criteria: - Must be able to speak English or Spanish and provide informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
PeACE
3 session peer coaching intervention
Community peer coaching
Peer coaching provided by community organizations that support the HBOC community

Locations

Country Name City State
United States Dana Farber Cancer Center Boston Massachusetts
United States University of Texas Southwestern Medical Center Dallas Texas
United States Hackensack University Medical Center Hackensack New Jersey
United States Memorial Sloan Kettering Cancer Center New York New York
United States University of Washington Seattle Washington
United States Georgetown University Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Georgetown University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cancer-related distress Cancer-related distress about hereditary breast and ovarian cancer risk at 12 months, gathered via self-report using the Impact of Events Scale, a 15 item measure scored on a 0-3 scale (0-45) with higher scores meaning higher distress 12 months
Primary Decisional conflict Decisional conflict about hereditary breast and ovarian cancer risk management decisions at 12 months gathered via self-report using the Decisional Conflict Scale. The 16 items on a 0-4 scale are summed, divided by 16 and multiplied by 25 for a total score (range=0-100); higher scores indicate higher conflict 12 months
Primary Genetic counseling Genetic counseling uptake at 12 months gathered via self-report (for untested women); this is a binary yes/no question 12 months
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