Choose to Lose for Women-Weight Loss to Reduce Breast Cancer Risk Factors
NCT ID: NCT01096901
Last Updated: 2015-10-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
EARLY_PHASE1
19 participants
INTERVENTIONAL
2010-11-30
2011-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Comprehensive behavioral weight loss
The group will be implemented to induce a 6% weight loss over 3 months. The lessons will follow protocols from the Look AHEAD trial and Diabetes Prevention Program. This behavioral program has been shown to promote long-term weight loss and a reduction in diabetes and cardiovascular risk factors, and is based on the social cognitive theory.
Behavioral Weight loss
Intervention groups will meet weekly for 12 weeks. Weekly meetings will focus on weight loss in women age 30-45 through behavioral weight loss topics. These topics are designed with the Look AHEAD protocols.
Education and Support Control group
Participants in this group will receive support and education about healthy eating and activity with lessons based on the Look AHEAD support and education control condition. Participants will attend monthly closed group meetings and meetings will be designed to promote retention but not weight loss.
No interventions assigned to this group
Interventions
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Behavioral Weight loss
Intervention groups will meet weekly for 12 weeks. Weekly meetings will focus on weight loss in women age 30-45 through behavioral weight loss topics. These topics are designed with the Look AHEAD protocols.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
30 Years
45 Years
FEMALE
Yes
Sponsors
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California Polytechnic State University-San Luis Obispo
OTHER
Responsible Party
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Suzanne Phelan
Principal Investigator
Principal Investigators
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Suzanne Phelan, PhD.
Role: PRINCIPAL_INVESTIGATOR
California Polytechnic State University-San Luis Obispo
Locations
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California Polytechnic State University
San Luis Obispo, California, United States
Countries
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Other Identifiers
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CP-EFI
Identifier Type: -
Identifier Source: secondary_id
CP-CTL
Identifier Type: -
Identifier Source: org_study_id
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