Connected Health Care in Exercise Program for Obesity
Study Details
Study Description
Brief Summary
Many kinds of wearable technology have become available, but the superiority of those devices in weight loss compared to the standard care without them is uncertain. The possible problems are long-term self-motivation, utility and validity of the device, and outcome measures in clinical trials. The connected health care with motivational interviewing as an intervention, and body composition parameters in addition to body weight as outcome measures are employed in the project. The expected outcome is that connected health care, which is more individualized approach by heath care professionals, is more effective compared to self-monitoring using wearable devices. Two types of wearable device are going to be used to monitor 1) body activity and 2) heart rate variables during exercise which reflect fitness level in this study in order to investigate appropriate monitoring parameters to predict outcome measures.
The hypothesis is that addition of connected health system will result in improvement of body composition and fitness level compared to self-monitoring.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
Patients with age 18 to 59 years old and body mass index between 30 to 39.9 are to be enrolled at Mayo Clinic in Arizona. All enrolled subjects receive wearable monitoring devices with remote tracking capability and brochure regarding nutrition and physical exercise with basic instruction. Subjects are randomly assigned to connected health care group versus self-monitoring group. Connected health care group will have 2 interviews about physical exercise and 6 communications with individualized instruction and counseling of their exercise including the usage of the monitoring devices. Self-monitoring group will do physical exercise following the initial basic instruction and self-monitor them.
All subjects visit Mayo Clinic to get outcome measures at 0, 12, and 24weeks. Outcome measures will be compared before, at 12 weeks, and after the 24 weeks of the fitness program.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Connected Health This group will get 2 interviews about physical exercise (exercise instruction with motivational interview) and 6 communications with individualized instruction and counseling of their physical exercise (investigators can access activity data and exercise log) including the usage of the monitoring device. |
Behavioral: Exercise instruction with motivational interview
An activity tracker and a heart rate monitor to track the participants activity and exercise records will be used. In addition to the basic instruction of exercise and nutrition, an exercise physiologist provides individualized exercise instruction with a motivational interviewing skill, which is a different style from traditional persuasive style of communication between the healthcare professionals and patients.
|
| Active Comparator: Self-Monitoring This group will do physical exercise following the initial instruction and self-monitor them. Investigators can access activity data and exercise log but will not discuss with the subjects about the data. |
Behavioral: Self-monitoring
An activity tracker and a heart rate monitor to track the participants activity and exercise records will be used. Basic instruction about exercise and nutrition is provided at the initial visit.
|
Outcome Measures
Primary Outcome Measures
- Change in Waist circumference [Baseline and 24 weeks]
Waist circumference is measured by tape at the end expiration while the patient is standing. Units centimeters.
Secondary Outcome Measures
- Change in weight [Baseline and 24 weeks]
Weight is measured using a commercially available body weight scale (TANITA body composition monitors). Units kg.
- Change in body fat percentage [Baseline and 24 weeks]
Body fat percentage is measured using a commercially available body fat scale (TANITA body composition monitors). Units percentage.
- Change in physical activity score [Baseline and 24 weeks]
International Physical Activity Questionnaire is filled out by patients. The International Physical Activity Questionnaire Long Form (IPAQ) (www.ipaq.ki.se) is to assess levels and patterns of physical activity. Continuous score expressed as "MET (metabolic equivalent)-min/week: MET level*minutes of activity/day*days per week" is calculated. Higher number means higher level of physical activity that a subject performed during last 7 days. The estimated range is from 0 to 3000. Units MET-minutes.
- Change in Physical Activity Vital Sign [Baseline and 24 weeks]
Physical Activity Vital Sign (PAVS) (Greenwood JL, 2010) is a short physical activity assessment using closed ended questions to ask how many days a subject performed physical activity during the past week. Higher number means a subject spent more days on performing physical activity. The range is from 0 to 7. Units days.
- Change in Veterans Specific Activity Questionnaire [Baseline and 24 weeks]
Veterans Specific Activity Questionnaire (VASQ) (Myers J, 2001) is a brief self administered questionnaire to predict exercise capacity (METs, metabolic equivalents). A subject select the minimum activity level that cause fatigue, short of breath, or discomfort. Higher number means higher fitness level of a subject. the range is from 1 to 13. Units METs.
- Change in heart rate variables [Baseline and 24 weeks]
Heart rate recovery after 6 minute walk test is evaluated. Units beats/minute.
- Change in 6 minute walk test [Baseline and 24 weeks]
Walking distance is evaluated. Units meters.
Eligibility Criteria
Criteria
Inclusion Criteria:
- Body Mass Index of 30 to <40 kg/m^2
Exclusion Criteria:
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End of organ damage from hypertension
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Diabetes
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Liver disease
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Chronic lung disease
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Neuromuscular disease
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Any conditions that limit exercise
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Currently involved in other weight program
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Mayo Clinic in Arizona | Scottsdale | Arizona | United States | 85259 |
Sponsors and Collaborators
- Mayo Clinic
- Arizona State University
Investigators
- Principal Investigator: Regis I Fernandes, Mayo Clinic
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 17-004529