Empowering African American cancer survivors through physical activity
Physical Activity Intervention Co-created and Tested With African American Colorectal Cancer Survivors
This study is testing a new physical activity program to see if it can help African American colorectal cancer survivors feel better and improve their quality of life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 72 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | UNC Lineberger Comprehensive Cancer Center Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Chapel Hill, North Carolina) |
| Trial ID | NCT06411756 on ClinicalTrials.gov |
What this trial studies
This research tests the feasibility of a physical activity intervention designed for African American individuals diagnosed with colorectal cancer. The intervention aims to improve the quality of life for underserved cancer survivors by increasing their physical activity levels. The study will recruit 72 participants and measure feasibility through various metrics such as reach, effectiveness, adoption, implementation, and maintenance, using the RE-AIM framework. Data will be collected at baseline and at 3 and 9 months to assess changes and the sustainability of the intervention's effects.
Who should consider this trial
Good fit: Ideal candidates for this study are African American individuals aged 18 and older who have been diagnosed with colorectal cancer and are scheduled to receive chemotherapy.
Not a fit: Patients who do not identify as African American or who have contraindications to unsupervised physical activity may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly enhance the quality of life for African American colorectal cancer survivors by promoting physical activity.
How similar studies have performed: Other studies have shown success with physical activity interventions for cancer survivors, particularly in improving quality of life, making this approach promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. self-identifying as AA of Black, 2. diagnosis of CRC, 3. scheduled to receive chemotherapy, 4. age 18 years or older, 5. no contraindications to unsupervised PA as determined by the PA readiness questionnaire, 6. oncologist approval to participate, and 7. a smartphone for Fitbit syncing.
Where this trial is running
Chapel Hill, North Carolina
- University of North Carolina at Chapel Hill — Chapel Hill, North Carolina, United States (Recruiting)
Study contacts
- Principal investigator: Rachel Hirschey, Ph.D, RN — UNC Lineberger Comprehensive Cancer Center
- Study coordinator: Cason E Whitcomb
- Email: cason_whitcomb@med.unc.edu
- Phone: 919-966-3036
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.