Promoting Activity in Cancer Survivors
Status: | Recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/2/2019 |
Start Date: | December 4, 2017 |
End Date: | December 2019 |
Contact: | Chad Rethorst, PhD |
Email: | chad.rethorst@utsouthwestern.edu |
Phone: | 2146480153 |
A randomized multi-component physical activity intervention for breast cancer survivors.
The research project is a study to assess the effects of a multi-component intervention in
increasing physical activity among breast cancer survivors. Individuals meeting
inclusion/exclusion criteria will be randomized to one of sixteen intervention groups for the
6 months. Intervention components will include print-based education, self-monitoring, Active
Living counseling, supervised exercise sessions, and facility access. Blood samples will be
collected at baseline. Assessments (anxiety, stress, sleep) and sample collection will also
occur at 3 time points during the intervention (Weeks 13 and 25). Changes in physical
activity will be assessed for each intervention group.
increasing physical activity among breast cancer survivors. Individuals meeting
inclusion/exclusion criteria will be randomized to one of sixteen intervention groups for the
6 months. Intervention components will include print-based education, self-monitoring, Active
Living counseling, supervised exercise sessions, and facility access. Blood samples will be
collected at baseline. Assessments (anxiety, stress, sleep) and sample collection will also
occur at 3 time points during the intervention (Weeks 13 and 25). Changes in physical
activity will be assessed for each intervention group.
Inclusion Criteria:
- breast cancer survivors between 3 months and 5 years post-treatment
- report <150 minutes of moderate-to-vigorous physical activity (MVPA) on the GPAQ
- physically able to engage in physical activity
Exclusion Criteria:
- medical condition contraindicating physical activity participation
- cognitively unable to give informed consent
We found this trial at
1
site
2201 Inwood Rd
Dallas, Texas 75235
Dallas, Texas 75235
(214) 645-8300
Principal Investigator: Madhukar Trivedi, MD
Phone: 214-648-0153
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