Weight management program for breast cancer survivors in rural communities

Development and Pilot Testing of a Novel Intervention to Reduce Cardiovascular Disease Risk Among Breast Cancer Survivors Living in Rural, Medically Underserved Communities

Not applicable Interventional Duke University · NCT07426952

This program will test whether a 12-week remote WeCan-Rural program helps rural breast cancer survivors with obesity lose weight, ease symptoms, and lower heart disease risk.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment40 (estimated)
Ages18 Years and up
SexFemale
SponsorDuke University Academic / other
Locations3 sites (Henderson, North Carolina and 2 other locations)
Trial IDNCT07426952 on ClinicalTrials.gov

What this trial studies

This randomized pilot will enroll 40 rural-dwelling women who completed stage I–III breast cancer treatment within the past five years and have a BMI >30. Participants are randomly assigned to the 12 weekly one-hour Zoom WeCan-Rural sessions or usual care, and receive tools such as an activity tracker, scale, and blood pressure monitor. Study visits occur twice about 12 weeks apart for weight, blood pressure, blood sample collection, and a short walking test, and participants complete online surveys on diet, activity, symptoms, and self-management confidence. Primary aims focus on feasibility (recruitment, retention, acceptability) and preliminary effects on weight, symptoms, physical activity, diet, and health self-efficacy.

Who should consider this trial

Good fit: Adult biological females (≥18 years) with stage I–III breast cancer who finished curative-intent treatment within five years, live in rural areas, have BMI >30, can do home-based activity, and can read/speak English are ideal candidates.

Not a fit: People with severe visual, hearing, cognitive impairment, severe mental illness that prevents participation, those who cannot use English-language remote delivery, or those unable to perform home-based activity are unlikely to benefit from this program.

Why it matters

Potential benefit: If successful, the program could help rural breast cancer survivors lose weight, reduce lingering symptoms, and lower cardiovascular risk through a convenient remote format.

How similar studies have performed: Previous lifestyle and remote weight-management programs for cancer survivors have shown feasibility and modest improvements in weight, activity, and symptoms, so this builds on existing evidence rather than being entirely novel.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* aged 18 years or older
* female (biological sex)
* diagnosis of stage I-III breast cancer
* completed treatments with curative intent (with the exception of hormonal treatments) in the last 5 years
* body mass index \>30
* healthy enough to participate in home-based physical activity
* able to speak/read English
* reports rating of ≥4 (i.e., moderate or more severe) out of 10 for one or more of the following symptoms at its worst in the last month (per the MD Anderson Symptom Inventory): pain, fatigue, sadness, and/or distress

Exclusion Criteria:

* visual, hearing or cognitive impairment or severe mental illness interfering with participation

Where this trial is running

Henderson, North Carolina and 2 other locations

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Breast Cancer SurvivorshipWeight ManagementCardiovascular RiskBreast Cancer
Last reviewed 2026-06-13 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.