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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States
Ability to recruit breast cancer survivors into a six-month breast cancer rehabilitation program
Time frame: Approximately 24 months
BMI
Time frame: 6 months
Muscular strength
Time frame: 6 months
Range of motion
Time frame: 6 months
Quality of life
Time frame: 6 months
Proportion of screened women who are eligible for the study and the proportion of eligible women who agree to participate
Time frame: Approximately 24 months
Proportion of women who complete the study and the average number of weeks of participation
Time frame: Approximately 24 months
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