Community exercise and nutrition program for cancer survivors
Feasibility of a Community-Based Cancer Survivor Exercise and Nutrition Education Program: Effects on Self-Efficacy, Quality of Life and Functional Performance
NA · Roswell Park Cancer Institute · NCT06565260
This study is testing a 12-week exercise and nutrition program to see if it can help cancer survivors feel healthier and improve their quality of life.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Roswell Park Cancer Institute (other) |
| Locations | 1 site (Buffalo, New York) |
| Trial ID | NCT06565260 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the feasibility and effectiveness of a 12-week supervised community-based exercise and nutrition program aimed at improving the physical activity and dietary habits of cancer survivors. Participants engage in aerobic and resistance exercises twice a week, along with weekly nutrition education sessions. The study also assesses changes in exercise self-efficacy, functional performance, and quality of life. Data collected will help determine the program's impact on survivors' overall health and well-being.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and older who have completed cancer treatment and are looking to improve their physical health.
Not a fit: Patients with uncontrolled illnesses, orthopedic disorders, or those currently on steroids may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could enhance the physical fitness and quality of life for cancer survivors.
How similar studies have performed: Other studies have shown positive outcomes with similar community-based exercise and nutrition interventions for cancer survivors.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years. * Have had a previous cancer diagnosis and completed all therapy OR are a caregiver for a patient who has had a previous cancer diagnosis. * Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related interventions. Exclusion Criteria: * Have uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia including atrial fibrillation (AFIB), multiple myeloma, or psychiatric illness/social situations that would limit compliance with study requirements. * Have orthopedic or neuromuscular disorders or arthritis that preclude participation in exercise. * Are pregnant or nursing. * History of a stem cell transplant. * Currently on steroids. * Unwilling or unable to follow protocol requirements. * Any condition which in the investigator's opinion deems the participant an unsuitable candidate to participate in the study.
Where this trial is running
Buffalo, New York
- Roswell Park Cancer Institute — Buffalo, New York, United States (RECRUITING)
Study contacts
- Principal investigator: Andrew D Ray — Roswell Park Cancer Institute
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.
Conditions: Hematopoietic and Lymphatic System Neoplasm, Malignant Solid Neoplasm