The purpose of this pilot study is to test a supervised exercise program for adults with a history of breast or gynecologic cancer to see if it is safe, helpful, and easy to take part in.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Recruitment rate calculated as the number of participants enrolled divided by the number approached or referred over the study period.
Timeframe: Recruitment period which will start at day 1 through two months
Retention rate defined as the proportion of enrolled participants who complete the 12-week intervention and post-intervention assessment.
Timeframe: Pre-assessment/treatment initiation through post-intervention assessment, approximately 14 weeks
Adherence to exercise sessions calculated as the number of completed supervised exercise sessions divided by the number of prescribed sessions.
Timeframe: Pre-assessment/treatment initiation through post-intervention assessment, approximately 14 weeks
Completeness of functional testing procedures defined as the proportion of participants with complete baseline and follow-up fitness assessments.
Timeframe: Pre-assessment/treatment initiation through post-intervention assessment, approximately 14 weeks