Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Post-treatment support program to help Black women breast cancer survivors in Western New York transition into survivorship

Official title: Thriving Beyond Breast Cancer: Post-Treatment Supportive Services Programming for Breast Cancer Survivors to Optimize Health During Survivorship

Run by Roswell Park Cancer Institute · NCT06833255 · Data updated 2026-11-12

This program tries group sessions and one-on-one peer mentoring to help Black women breast cancer survivors in Western New York adjust to life after finishing treatment.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment125 (estimated)
SponsorRoswell Park Cancer Institute
Academic / other
Drugs / interventionsradiation
Locations1 site (Buffalo, New York)
StatusRecruiting
StartedApril 21, 2025
Main results expectedMarch 30, 2030
Study endsNovember 30, 2030
Registry record updatedNovember 24, 2025
Trial IDNCT06833255 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults living in Western New York who have completed primary breast cancer treatment are eligible, with priority for Black/African American women and those within one year of treatment completion.

Probably not a fit

Patients who are still undergoing primary cancer treatments, who live far from Western New York, or who cannot attend regular in-person sessions are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The program delivers no-cost, culturally tailored survivorship support to up to 100 breast cancer survivors in Western New York, prioritizing those who are African American and those within one year of completing primary treatment. Participants join two-hour group sessions on the 1st and 3rd Thursdays of each month and meet with a long-term survivor mentor for one-on-one sessions on the 2nd and 4th Thursdays for up to 12 months. Mentors support monthly self-assessments, help identify and address modifiable risk factors, and connect mentees to local resources and providers as needed. The project will measure feasibility, acceptability, participant quality of life, and factors affecting sustainability and potential spread to other National Witness Project® sites.

Why it matters

Potential benefit: If successful, the program could improve survivors' social support, quality of life, and self-management during the critical first year after treatment.

How similar studies have gone: Peer mentoring and group-support programs for breast cancer survivors have shown moderate success in improving quality of life and follow-up behaviors, so this approach builds on existing, partly validated models.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Ability to speak and read English
* At least 18 years of age or older
* Live in the Western New York area
* Has been diagnosed with breast cancer (any stage)
* Has completed primary breast cancer treatments (i.e., systemic, radiation, and/or surgical interventions other than breast reconstruction surgeries)

  * Mentors are at least one-year post-treatment completion
  * Mentees are less than one-year post-treatment completion
  * Note: Individuals who have completed primary breast cancer treatments who are being managed with ongoing hormonal therapies and/or are awaiting breast reconstruction surgery may participate in this study (i.e., these therapies do not meet exclusion criteria)

    * Note: Although any breast cancer survivor may participate, priority will be given to those who have most recently transitioned into their post-treatment life (or those who report that support was either not offered or was unavailable to them during their less recent transition into post-treatment life) and /or self-identify as African American

Exclusion Criteria:

* Currently receiving neoadjuvant and/or adjuvant systemic and/or radiations therapies
* Unwilling or unable to complete the assessment in English
* Are pregnant or nursing
* Are unwilling or unable to follow protocol requirements

  * Note: Individuals who have completed primary breast cancer treatments who are being managed with ongoing hormonal therapies and/or are awaiting breast reconstruction surgery may participate in this study (i.e., these therapies do not meet exclusion criteria)

Where it's running

  • Roswell Park Cancer Institute
    Buffalo, New York, United States
    Recruiting

Study contacts

  • Principal investigator: Julia Devonish — Roswell Park Cancer Institute

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.