Breast Cancer Clinical Trial
Choose to Lose for Women-Weight Loss to Reduce Breast Cancer Risk Factors
Summary
This study is investigating the changes in specific hormone levels in women age 30-45 after a 12 week weight loss intervention.
Full Description
In sum, excess body weight and inactivity have emerged as strong avoidable causes of postmenopausal breast cancer, with the greatest potential for primary prevention occurring during the premenopausal years. However, surprisingly, no study to date has examined the effects of a standard behavioral weight loss intervention on breast cancer risk markers in premenopausal women. Understanding the effects of weight loss in premenopausal women is a critical next step in existing research and will inform the development of future breast cancer primary prevention programs. The purpose of this study is to determine the feasibility of recruiting, treating, and retaining 20 overweight/obese women in a 12-week randomized control trial examining feasibility and effects of a behavioral weight loss program on breast cancer risk markers in premenopausal women. Participants will be randomly assigned to either a 12-week comprehensive behavioral weight loss program (n=10) or control condition (n=10). All women will be assessed at baseline and after 3 months of treatment.
Eligibility Criteria
Inclusion Criteria:
Premenopausal women
Age 30-45
Current BMI of >25
English or Spanish speaking
5th grade reading level
Menstrual regularity, defined as menstrual cycle length of 27-31 and < 1 missed period within the past 12 months.
Exclusion Criteria:
Current use or recent (< 6 months) use of oral contraceptives, hormones, or other hormone-influencing medications
Pregnant, lactating or planning pregnancy in the next 12 weeks
Unwilling and able to location for intervention visits.
Serious medical condition requiring the supervision of a physician for exercise and diet
History of eating disorder
History of or current use of drugs
Current treatment for serious psychological disorder
Donation of blood within past 6 weeks.
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There is 1 Location for this study
San Luis Obispo California, 93407, United States
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