Connected Health Care in Exercise Program for Obesity
Primary Purpose
Obesity, Physical Activity, Exercise
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise instruction with motivational interview
Self-monitoring
Sponsored by

About this trial
This is an interventional prevention trial for Obesity focused on measuring Obesity, Physical Activity, Exercise, Wearable device
Eligibility Criteria
Inclusion Criteria:
- Body Mass Index of 30 to <40 kg/m^2
Exclusion Criteria:
- End of organ damage from hypertension
- Diabetes
- Liver disease
- Chronic lung disease
- Neuromuscular disease
- Any conditions that limit exercise
- Currently involved in other weight program
Sites / Locations
- Mayo Clinic in Arizona
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Connected Health
Self-Monitoring
Arm Description
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.
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.
Outcomes
Primary Outcome Measures
Change in Waist circumference
Waist circumference is measured by tape at the end expiration while the patient is standing. Units centimeters.
Secondary Outcome Measures
Change in weight
Weight is measured using a commercially available body weight scale (TANITA body composition monitors). Units kg.
Change in body fat percentage
Body fat percentage is measured using a commercially available body fat scale (TANITA body composition monitors). Units percentage.
Change in physical activity score
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
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
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
Heart rate recovery after 6 minute walk test is evaluated. Units beats/minute.
Change in 6 minute walk test
Walking distance is evaluated. Units meters.
Full Information
NCT ID
NCT03446235
First Posted
January 11, 2018
Last Updated
January 22, 2019
Sponsor
Mayo Clinic
Collaborators
Arizona State University
1. Study Identification
Unique Protocol Identification Number
NCT03446235
Brief Title
Connected Health Care in Exercise Program for Obesity
Official Title
Feasibility and Explorative Study to Test the Superiority of Connected Health Care Using Wearable Device to Improve Body Composition and Fitness Level
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
December 4, 2017 (Actual)
Primary Completion Date
August 31, 2018 (Actual)
Study Completion Date
August 31, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
Collaborators
Arizona State University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. 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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Physical Activity, Exercise
Keywords
Obesity, Physical Activity, Exercise, Wearable device
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
19 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Connected Health
Arm Type
Experimental
Arm Description
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.
Arm Title
Self-Monitoring
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Exercise instruction with motivational interview
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Self-monitoring
Intervention Description
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.
Primary Outcome Measure Information:
Title
Change in Waist circumference
Description
Waist circumference is measured by tape at the end expiration while the patient is standing. Units centimeters.
Time Frame
Baseline and 24 weeks
Secondary Outcome Measure Information:
Title
Change in weight
Description
Weight is measured using a commercially available body weight scale (TANITA body composition monitors). Units kg.
Time Frame
Baseline and 24 weeks
Title
Change in body fat percentage
Description
Body fat percentage is measured using a commercially available body fat scale (TANITA body composition monitors). Units percentage.
Time Frame
Baseline and 24 weeks
Title
Change in physical activity score
Description
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.
Time Frame
Baseline and 24 weeks
Title
Change in Physical Activity Vital Sign
Description
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.
Time Frame
Baseline and 24 weeks
Title
Change in Veterans Specific Activity Questionnaire
Description
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.
Time Frame
Baseline and 24 weeks
Title
Change in heart rate variables
Description
Heart rate recovery after 6 minute walk test is evaluated. Units beats/minute.
Time Frame
Baseline and 24 weeks
Title
Change in 6 minute walk test
Description
Walking distance is evaluated. Units meters.
Time Frame
Baseline and 24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Body Mass Index of 30 to <40 kg/m^2
Exclusion Criteria:
End of organ damage from hypertension
Diabetes
Liver disease
Chronic lung disease
Neuromuscular disease
Any conditions that limit exercise
Currently involved in other weight program
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Regis I Fernandes
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic in Arizona
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Connected Health Care in Exercise Program for Obesity
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