Communication & Peer Support Effects on Physical Activity in Overweight Postmenopausal Women (BePHIT)
Healthy, Obesity, Postmenopausal

About this trial
This is an interventional prevention trial for Healthy focused on measuring Feasibility study, Interactive voice response system (IVR), health coach, no evidence of disease
Eligibility Criteria
Inclusion Criteria:
- Present a letter/documentation from a primary physician stating that they can participate in a physical activity program that will require walking up to 10,000 steps per day
- Have a body mass index (BMI) between 25 and 40 kg/m^2 (inclusive)
- Be postmenopausal, defined as no period for 12 months if over age 55, or no period for 12 months; also, women who have had their ovaries removed will be considered as postmenopausal
- Willing to participate in a wellness program that lasts 12 weeks and involves walking for at least 30 minutes a day on most days
- Has access to a cell phone during the 12-week intervention
- Functional knowledge of English (ability to both read and write)
Exclusion Criteria:
- Taking hormone replacement therapy within 3 months of enrollment
- Taking Tamoxifen or Raloxifene within 3 months of enrollment
- Enrolled in a weight management program, such as Weight Watchers
- Engaged in regular, planned walking of at least 30 minutes a day
- Previous history of breast cancer
- Premenopausal
- Age > 75 years, to minimize co-morbidities
- Cannot walk one mile
Sites / Locations
- Ohio State University Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Arm I (health coach)
Arm II (no coach condition)
Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system and from a health coach. Participants in this arm of the study, interacted with the IVR system and had the option of interacting with the health coach.
Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system. Participants in this arm of the study only interacted with the IVR system.