Recruiting
Social and Environmental Determinants of Breast Cancer Survivorship: the Black Breast Cancer Survivor's Intervention (BBCSI)
The goal of this research study is to learn about the effects of the BBCSI course on the quality of life of Black breast cancer survivors. A community-based and peer-led Black Breast Cancer Survivor's Intervention (BBCSI) course has been developed to help improve the quality of life of Black breast cancer survivors.
ClinicalTrials.gov IDNCT06885203
PhaseNA
Enrollment56
SponsorM.D. Anderson Cancer Center
Age18 Years
SexFEMALE
Conditions studied
Breast Cancer
About this study
The goal of this research study is to learn about the effects of the BBCSI course on the quality of life of Black breast cancer survivors. A community-based and peer-led Black Breast Cancer Survivor's Intervention (BBCSI) course has been developed to help improve the quality of life of Black breast cancer survivors.
Interventions
- Behavioral: Black Breast Cancer Survivor's Intervention — Participants will complete the BBCSI course (1-hour virtual sessions every week for 6 weeks), answer questionnaires before and after the course, and provide urine samples.
Primary outcomes
- Safety and Adverse Events (AEs) (Time Frame: Through study completion; an average of 1 year)
Eligibility information
Inclusion Criteria:
Master Trainers:
To be eligible to participate in this study, an individual must meet all the following criteria:
1. Adult women aged 18 years and older
2. Histologically confirmed stage 0-III breast cancer
3. No evidence of metastatic disease
4. Self-identify as Black
5. Able to communicate in English
Participants:
To be eligible to participate in this study, an individual must meet all the following criteria:
1. Adult women aged 18 years and older
2. Histologically confirmed stage 0-III breast cancer
3. No evidence of metastatic disease
4. Self-identify as Black
5. Able to communicate in English
Community Interventionists:
To be eligible to participate in this study, an individual must meet all the following criteria:
1. Adult women aged 18 years and older
2. Histologically confirmed stage 0-III breast cancer
3. No evidence of metastatic disease
4. Self-identify as Black
5. Former study participants that have completed the intervention
6. Able to communicate in English
General Exclusion Criteria:
1. Men or woman below 18 years of age
2. Does not have a histologically confirmed breast cancer
3. There's evidence of metastatic disease
4. Does not self-identify as Black
5. Unable to communicate in English
Additional Exclusion Criteria - Community Interventionists
1\. Has not previously participated in and completed the study intervention as a participant
Study locations
- The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030 United States
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.