Breast Cancer Rehabilitation Program in Improving Quality of Life in Breast Cancer Survivors
Status: | Active, not recruiting |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/3/2017 |
Start Date: | June 2010 |
End Date: | October 2017 |
A Pilot Study to Evaluate the Feasibility of a Breast Cancer Rehabilitation Program in Survivors of Breast Cancer
RATIONALE: A breast cancer rehabilitation program and exercise therapy may help improve the
quality of life of breast cancer survivors.
PURPOSE: This clinical trial studies a breast cancer rehabilitation program in improving
quality of life in breast cancer survivors.
quality of life of breast cancer survivors.
PURPOSE: This clinical trial studies a breast cancer rehabilitation program in improving
quality of life in breast cancer survivors.
PRIMARY OBJECTIVES:
I. To estimate accrual, retention, adherence, and participation of breast cancer survivors to
a breast cancer rehabilitation program.
II. To estimate the variability of weight, six-minute walk, quality of life and other
psychosocial and physical measures in women participating in the BCRP.
SECONDARY OBJECTIVES:
I. To assess changes in the anthropometric, psychosocial, and physical outcomes over the
six-month period of the BCRP.
II. To document the types and the rates of adverse events associated with the BCRP.
OUTLINE:
Patients attend exercise therapy sessions over 1 hour 3 times a week for 6 months. Exercise
therapy sessions are comprised of a 10 minute warm-up of light stretching and aerobic type
exercise (walking, cycling), 30 minutes of endurance type exercise (cycle, walking), and 20
minutes of resistance training exercise.
I. To estimate accrual, retention, adherence, and participation of breast cancer survivors to
a breast cancer rehabilitation program.
II. To estimate the variability of weight, six-minute walk, quality of life and other
psychosocial and physical measures in women participating in the BCRP.
SECONDARY OBJECTIVES:
I. To assess changes in the anthropometric, psychosocial, and physical outcomes over the
six-month period of the BCRP.
II. To document the types and the rates of adverse events associated with the BCRP.
OUTLINE:
Patients attend exercise therapy sessions over 1 hour 3 times a week for 6 months. Exercise
therapy sessions are comprised of a 10 minute warm-up of light stretching and aerobic type
exercise (walking, cycling), 30 minutes of endurance type exercise (cycle, walking), and 20
minutes of resistance training exercise.
Inclusion
- First occurrence of breast cancer
- BMI >= 25
- Recently completed treatment(chemotherapy/radiation) for breast cancer (=< 8 weeks),
but can be receiving adjuvant hormonal therapy
- Willing to comply with study visits, as outlined in the protocol
- Lives within 30 miles of study site, or willing to travel to study site if outside a
30-mile radius
- Ability to participate in a moderate exercise program, such as freedom from any
orthopedic abnormalities that would prevent participation
- Ability to understand and the willingness to sign a written informed consent document
Exclusion
- Unstable angina
- Cardiac conduction disturbances
- Plans to move from the study area
- Dementia that is medically documented or suspected
- Advanced arterial disease causing ischemia of any limb
- Physical immobility
- Homebound for medical reasons
- Dependent on wheelchair for mobility
- Chronic disease which significantly reduces 4-year survival
- Recurrent breast cancer
We found this trial at
1
site
1 Medical Center Blvd
Winston-Salem, North Carolina 27157
Winston-Salem, North Carolina 27157
336-716-2011
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