Effect of the LIVESTRONG at the YMCA Exercise Program on Cancer Related Outcomes in Cancer Survivors
Completed · Phase 3
Conditions studied: Breast Cancer
In brief
The proposed study is a randomized trial evaluating the impact of the 12-week LIVESTRONG exercise program vs. waitlist control on cancer-related outcomes in 200 cancer survivors.
Key facts
- Study ID
- NCT02112149
- Run by
- Yale University
- People needed
- 200
- Starts
- 2013-02-01
- Expected to finish
- 2015-12-01
- Last updated by the study team
- 2016-07-13
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Cancer diagnosis excluding non-melanoma skin cancer
- Physically able to exercise
- Able to complete forms and understand instructions in English
- Agrees to be randomly assigned to either exercise or wait-list control group
- Willing and able to attend one of the LIVESTRONG at the YMCA programs for 12 weeks
- Willing and able to complete the baseline and 3-month clinic visits
You may not qualify if…
- > 80 years of age
- < 18 years of age
- Recent (past 6 months) stroke/myocardial infarction or congestive heart failure/documented ejection fraction < 40%
- Plans to undergo a major surgical procedure in the next 6 months
- Presence of dementia or major psychiatric disease that would preclude participation in a group-based exercise program
- Pregnant women or women intending to become pregnant
Where it is running
- Yale University — New Haven, Connecticut, United States
- Dana-Farber Cancer Institute — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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