Virtual exercise program for cancer survivors
A Randomized Controlled Trial Adding Behavioural Counselling to Supervised Physical Activity in Cancer Survivors
NA · University of Toronto · NCT06624930
This study is testing whether a 6-month virtual exercise program can help cancer survivors be more active and improve their quality of life.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 236 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Toronto (other) |
| Drugs / interventions | radiation |
| Locations | 1 site (Toronto, Ontario) |
| Trial ID | NCT06624930 on ClinicalTrials.gov |
What this trial studies
This trial examines the effects of a virtual 6-month supervised physical activity program combined with either standard exercise counseling or motivationally-enhanced behavioral counseling on cancer survivors. The study aims to increase moderate to vigorous physical activity levels in participants, addressing long-term side effects of cancer treatment such as fatigue and depression. Participants will be followed up at 6 months and 1 year post-intervention to assess the sustainability of behavior change and improvements in quality of life. The intervention is designed based on evidence from exercise oncology and behavior change techniques.
Who should consider this trial
Good fit: Ideal candidates are cancer survivors aged 18 and older who have completed primary treatment within the last 5 years and are currently physically inactive.
Not a fit: Patients with uncontrolled comorbidities or medical conditions that prohibit physical activity may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve the physical activity levels and overall quality of life for cancer survivors.
How similar studies have performed: Other studies have shown success with virtual exercise interventions for cancer survivors, indicating a promising approach to improving physical activity and health outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥18 years of age * Confirmed diagnosis of cancer of any type (Stages I to III; localized) * Have completed primary cancer treatment within 5 years * At least 12 weeks after surgery completion * At least 6 weeks after radiation treatment * Proficient in English * Physically inactive (self-report less than 90 min of MVPA/week ) * Ambulate in daily life with minimal gait aid use * Access to a smartphone/tablet/computer with webcam for videoconferencing and a Bluetooth connection * Access to the internet * No cardiac contraindications (e.g., unstable angina, heart failure, coronary artery disease, diagnosed abnormality of heart rhythm) Exclusion Criteria: * A medical condition that prohibits PA (e.g., joint restriction or weight bearing precautions) * Uncontrolled comorbidities or cardiovascular contraindications that would increase risk associated with supervised and unsupervised exercise (e.g., cardiac contraindications, severe arthritis, recent fall within the last 6-12 months) * Presence of advanced cancer (i.e., Stage IV; metastatic) * Pregnancy * Do not intend to live in Canada for the next 18 months
Where this trial is running
Toronto, Ontario
- Exercise Oncology Lab - University of Toronto — Toronto, Ontario, Canada (RECRUITING)
Study contacts
- Principal investigator: Linda Trinh, PhD — University of Toronto
- Study coordinator: Linda Trinh, PhD
- Email: exercise.oncology@utoronto.ca
- Phone: 4169463624
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.