Home-based exercise program for endometrial cancer survivors in rural areas
RISE: Remote Intervention for Strength Training in Endometrial Cancer
This study tests a home-based exercise program to see if it can help endometrial cancer survivors in rural areas feel better and improve their physical health.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 50 Years and up |
| Sex | Female |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Trial ID | NCT06213571 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates a remote home-based exercise program designed to improve the quality of life for endometrial cancer survivors living in rural areas. The program includes resistance band and body weight exercises, along with educational materials and weekly coaching sessions over a 10-week period. The study aims to assess the recruitment, retention, and acceptability of this intervention, as well as its effectiveness on physical functioning in participants. By addressing barriers to exercise access, the trial seeks to provide a scalable solution for underserved populations.
Who should consider this trial
Good fit: Ideal candidates are adults aged 50 and older who are survivors of early stage, low risk endometrial cancer and reside in rural areas.
Not a fit: Patients with severe mobility impairments or those who do not speak English may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could enhance the quality of life and physical functioning for endometrial cancer survivors in rural areas.
How similar studies have performed: Other studies have shown promise in using remote exercise interventions for cancer survivors, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 50+ * Stage IA-IB endometrial cancer * Grade 1-2 disease * No recurrence documented * Internet access * Access to a remote device with a camera such as a computer, smartphone or tablet * \> 1 year but less than 5 years from surgery * Primary residence in rural-urban commuting area (RUCA) (rural-urban commuting area) codes 4.0 through 10.0 or of American Indian, Alaskan Native, Black or Hispanic background Exclusion Criteria: * Paraplegia/hemiplegia * No English speaking
Where this trial is running
Rochester, Minnesota
- Mayo Clinic in Rochester — Rochester, Minnesota, United States (Recruiting)
Study contacts
- Principal investigator: Amanika A Kumar, MD — Mayo Clinic in Rochester
- Study coordinator: Clinical Trials Referral Office
- Email: mayocliniccancerstudies@mayo.edu
- Phone: 855-776-0015
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.