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

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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.

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.

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
336-716-2011
Wake Forest University Health Sciences Welcome to Wake Forest Baptist Medical Center, a fully integrated...
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from
Winston-Salem, NC
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