BePHIT: Communication & Peer Support Effects on Physical Activity in Overweight Postmenopausal Women
Study Details
Study Description
Brief Summary
This randomized clinical trial studies the feasibility of tailored physical activity intervention that is administered using Interactive Voice Response technology and cell phones. Interactive voice response and health coach support may motivate overweight postmenopausal women to stick to their exercise regimen to reduce the risk of getting breast cancer.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
PRIMARY OBJECTIVES:
- To design, develop and test the feasibility of implementing a physical activity intervention using tailored communication and Interactive Voice Response (IVR) technology. We will to address four basic questions to accomplish this aim:
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Among overweight, postmenopausal women, who pass the screening criteria, what is the percentage of women who are willing to participate in a 12-week physical activity intervention that includes two 1-mile walk tests and two visits to the General Clinical Research Center (GCRC)?
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After beginning the study, what proportion of women use the cell phone and land line at least 5 days a week to get a physical activity intervention message?
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How many participants are enrolled and participating in the study at the end of the 12-week intervention period?
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On average, how many steps per day do participants walk? How many of the participants reach the 10,000 steps-per-day target by the end of the 12 week-intervention?
SECONDARY OBJECTIVES:
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The effectiveness (satisfaction, convenience, ease of operation) of all the materials and processes.
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Examine whether social support from a health coach results in improvements in our measures of adherence and satisfaction.
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Examine the correlation between self-reported steps per day with improvements in performance on a 1-mile walk test administered at the beginning and the end of the 12-week intervention.
OUTLINE: Patients are randomized to 1 of 2 treatment arms.
ARM I. COACH-CONDITION: Participants participate in a 12-week physical activity program (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.
ARM II: NO-COACH CONDITION: Participants participate in a 12-week physical activity program (walking program) administered using an IVR system.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Arm I (health coach) 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. |
Behavioral: communication intervention
Participants participate in a 12-week physical activity intervention (walking program)and receive health mail messages via IVR system and had the option of communicating with a health coach.
Behavioral: exercise intervention
Participants participate in a 12-week physical activity intervention administered using an IVR system.
|
| Active Comparator: Arm II (no coach condition) 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. |
Behavioral: exercise intervention
Participants participate in a 12-week physical activity intervention administered using an IVR system.
|
Outcome Measures
Primary Outcome Measures
- Change in time taken to complete a one mile walk. [12 weeks]
Secondary Outcome Measures
- Changes in anthropometrics, psychometrics and the benefits of a health coach. [12 weeks]
- Weekly effectiveness (satisfaction, convenience, ease of operation) of all the materials and processes as assessed by questionnaires. [12 weeks]
- If the self-reported steps per day, derived from daily activity logs, relates to the change in performance on the 1-mile walk test between baseline and end of study. [12 Week]
The steps walked per day and the change in performance on the 1-male walk test are both outcomes.
Eligibility Criteria
Criteria
Inclusion Criteria:
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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
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Have a body mass index (BMI) between 25 and 40 kg/m^2 (inclusive)
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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
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Willing to participate in a wellness program that lasts 12 weeks and involves walking for at least 30 minutes a day on most days
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Has access to a cell phone during the 12-week intervention
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Functional knowledge of English (ability to both read and write)
Exclusion Criteria:
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Taking hormone replacement therapy within 3 months of enrollment
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Taking Tamoxifen or Raloxifene within 3 months of enrollment
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Enrolled in a weight management program, such as Weight Watchers
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Engaged in regular, planned walking of at least 30 minutes a day
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Previous history of breast cancer
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Premenopausal
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Age > 75 years, to minimize co-morbidities
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Cannot walk one mile
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Ohio State University Medical Center | Columbus | Ohio | United States | 43210 |
Sponsors and Collaborators
- Ohio State University Comprehensive Cancer Center
- Breast Cancer Research Foundation
Investigators
- Principal Investigator: Electra Paskett, PhD, Ohio State University
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- OSU-05005
- NCI-2012-00204