Promoting Physical Activity Among Bariatric Surgery Patients
NCT ID: NCT01722357
Last Updated: 2020-06-11
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
NA
152 participants
INTERVENTIONAL
2009-11-30
2019-08-31
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
TREATMENT
NONE
Study Groups
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Pedometer + Exercise Counseling
Pedometer
Participants are provided with Omron Model HJ-151 pedometers and given instruction on how to use the pedometer to set goals for increasing physical activity. They are given diaries to track their daily step counts.
Exercise Counseling
Manualized cognitive behavioral treatment program including goal setting, adding exercise throughout the day, physical limitations/injuries, maintaining motivation, benefits of exercise, FITT principles, exercise as recreation, and restructuring thoughts related to activity.
Pedometer
Pedometer
Participants are provided with Omron Model HJ-151 pedometers and given instruction on how to use the pedometer to set goals for increasing physical activity. They are given diaries to track their daily step counts.
Usual Care
Self-help information provided on physical activity (WIN:Weight Control Network "Active At Any Size" provided by National Institute of Diabetes and Digestive and Kidney Diseases, 2006).
No interventions assigned to this group
Interventions
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Pedometer
Participants are provided with Omron Model HJ-151 pedometers and given instruction on how to use the pedometer to set goals for increasing physical activity. They are given diaries to track their daily step counts.
Exercise Counseling
Manualized cognitive behavioral treatment program including goal setting, adding exercise throughout the day, physical limitations/injuries, maintaining motivation, benefits of exercise, FITT principles, exercise as recreation, and restructuring thoughts related to activity.
Eligibility Criteria
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Inclusion Criteria
* Men and women 18 years and older
* The participant must be motivated to enroll in a study assessing physical activity before and after bariatric surgery, able to understand and comply with the study, and must agree to return for scheduled visits
* All participants must sign a written, informed consent
Exclusion Criteria
* Abnormal electrocardiogram (ECG), assessed at the pretreatment screening visit that the medically responsible investigator deems inappropriate for participation in a physical activity program.
* Unable to progress toward 30 minutes of continuous walking during the 6 months of study participation.
18 Years
ALL
No
Sponsors
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St. Vincent Foundation
OTHER
Ascension St. Vincent Carmel Hospital
OTHER
Responsible Party
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Principal Investigators
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David B Creel, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Vincent Carmel Hospital Bariatric Center of Excellence
Locations
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St. Vincent Carmel Hospital Bariatric Center of Excellence
Carmel, Indiana, United States
Countries
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References
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Creel DB, Schuh LM, Reed CA, Gomez AR, Hurst LA, Stote J, Cacucci BM. A randomized trial comparing two interventions to increase physical activity among patients undergoing bariatric surgery. Obesity (Silver Spring). 2016 Aug;24(8):1660-8. doi: 10.1002/oby.21548. Epub 2016 Jul 1.
Creel DB, Schuh LM, Newton RL Jr, Stote JJ, Cacucci BM. Exercise Testing Reveals Everyday Physical Challenges of Bariatric Surgery Candidates. J Phys Act Health. 2017 Dec 1;14(12):913-918. doi: 10.1123/jpah.2017-0128. Epub 2017 Oct 12.
Other Identifiers
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09110
Identifier Type: -
Identifier Source: org_study_id
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