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Breast Cancer Survivors: Exercise and Raloxifene
RATIONALE: Raloxifene and exercise may improve bone health and quality of life in breast cancer survivors. Assessing bone health and quality of life may improve the ability to plan treatment. PURPOSE: Randomized clinical trial to study the effectiveness of raloxifene with or without exercise compared with exercise alone in women who have been previously treated for breast cancer.
OBJECTIVES: * Determine the effects of raloxifene with or without exercise versus exercise alone on bone reabsorption rate, bone formation rate, and bone density in women previously treated for breast cancer. * Determine the effects of these regimens on the quality of life of these patients. OUTLINE: This is a randomized, placebo-controlled, multicenter study. Patients are randomized to one of four treatment arms. * Arm I: Patients are asked to exercise 5 days a week with instruction. Patients also receive oral placebo once daily. * Arm II: Patients receive oral raloxifene once daily. * Arm III: Patients are asked to exercise as in arm I. Patients also receive oral raloxifene once daily. * Arm IV: Patients receive oral placebo once daily. All patients receive oral calcium supplements once daily. Treatment continues in all arms for 24 months in the absence of disease progression or unacceptable toxicity. Quality of life is assessed at baseline and every 3 months during study. PROJECTED ACCRUAL: A total of 240 patients (60 per treatment arm) will be accrued for this study.
Age
All ages
Sex
FEMALE
Healthy Volunteers
No
OHSU Knight Cancer Institute
Portland, Oregon, United States
Start Date
March 1, 2001
Primary Completion Date
April 1, 2003
Completion Date
April 1, 2003
Last Updated
May 28, 2012
80
ACTUAL participants
raloxifene
DRUG
quality-of-life assessment
PROCEDURE
Lead Sponsor
OHSU Knight Cancer Institute
Collaborators
NCT05673200
NCT05372640
Data Source & Attribution
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