Actively Recruiting
A Post-treatment Supportive Service Program for the Transition Into Survivorship for Black Women Breast Cancer Survivors in Western New York
Led by Roswell Park Cancer Institute · Updated on 2025-11-24
125
Participants Needed
1
Research Sites
292 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial studies whether a post-treatment supportive service program can be used to help breast cancer survivors in Western New York (WNY) transition into post-treatment life (survivorship). The post-treatment supportive service program is delivered to breast cancer survivors of WNY. It combines group support sessions and one-on-one (1:1) peer mentoring sessions. The group support sessions include traditional support groups, educational topics/lessons, activities, such as cooking lessons, celebrations, or facility tours, and guest speakers. The 1:1 peer mentoring sessions are held with a long-term breast cancer survivor mentor. The long-term breast cancer survivor mentor helps the mentee get in the practice of performing once monthly self-assessments and create plans to help improve any identified modifiable risk factors. The long-term breast cancer survivor mentor can also help connect the mentee to providers or resources as needed. A post-treatment supportive service program may help Black women breast cancer survivors in WNY transition into survivorship.
CONDITIONS
Official Title
A Post-treatment Supportive Service Program for the Transition Into Survivorship for Black Women Breast Cancer Survivors in Western New York
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ability to speak and read English
- At least 18 years of age or older
- Live in the Western New York area
- Diagnosed with breast cancer at any stage
- Completed primary breast cancer treatments (systemic, radiation, and/or surgical interventions other than breast reconstruction)
- Mentors are at least one year post-treatment completion
- Mentees are less than one year post-treatment completion
- Individuals on ongoing hormonal therapies or awaiting breast reconstruction may participate
- Priority given to those recently transitioned into post-treatment life and/or self-identify as African American
You will not qualify if you...
- Currently receiving neoadjuvant and/or adjuvant systemic and/or radiation therapies
- Unable or unwilling to complete assessments in English
- Pregnant or nursing
- Unwilling or unable to follow protocol requirements
- Individuals on ongoing hormonal therapies or awaiting breast reconstruction are not excluded
AI-Screening
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Trial Site Locations
Total: 1 location
1
Roswell Park Cancer Institute
Buffalo, New York, United States, 14263
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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