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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2025-02122 | Other Identifier | NCI-CTRP Clinical Trials Registry |
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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.
Primary Objectives:
Develop a prototype of the BBCSI curriculum and assess satisfaction of the intervention.
Determine the preliminary efficacy of the BBCSI.
Evaluate fidelity, feasibility, acceptability, barriers, and facilitators of the BBCSI.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Immediate Intervention Group | Experimental | Participants will be recruited through our Community Based Organizations (CBOs) and other community collaborator networks. |
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| Wait-List (start in week 7) | Experimental | Participants will be recruited through our Community Based Organizations (CBOs) and other community collaborator networks. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Black Breast Cancer Survivor's Intervention | Behavioral | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Safety and Adverse Events (AEs) | Safety and Adverse Events (AEs) | Time Frame: Through study completion; an average of 1 year |
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Inclusion Criteria:
Master Trainers:
To be eligible to participate in this study, an individual must meet all the following criteria:
Participants:
To be eligible to participate in this study, an individual must meet all the following criteria:
Community Interventionists:
To be eligible to participate in this study, an individual must meet all the following criteria:
General Exclusion Criteria:
Additional Exclusion Criteria - Participants 1. More than four years of diagnosis
Additional Exclusion Criteria - Community Interventionists
1. Has not previously participated in and completed the study intervention as a participant
Gender identity
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dede Teteh-Brooks, DRPH | Contact | 713-563-3493 | dkteteh@mdanderson.org |
| Name | Affiliation | Role |
|---|---|---|
| Dede Teteh-Brooks, DRPH | M.D. Anderson Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The University of Texas M. D. Anderson Cancer Center | Recruiting | Houston | Texas | 77030 | United States |
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| Label | URL |
|---|---|
| MD Anderson Cancer Center Website | View source |
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
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| D017437 |
| Skin and Connective Tissue Diseases |