- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05123235
Effectiveness of a Telehealth-based Physical Activity Intervention
June 6, 2023 updated by: East Carolina University
The Effectiveness of a Telehealth-Based Physical Activity Intervention in Adolescents Receiving Treatment for Obesity
This study is a 11 week telehealth intervention focusing on increasing physical activity in adolescents who are receiving medical care for obesity.
The participants will be randomized into two groups: control and intervention.
During the 11 weeks both groups will be contacted once a week for a video call.
The control group will report their past week physical activity levels and the intervention group will review the material in weekly newsletters on behavior changes related to physical activity.
Physical activity levels will be measures before and after the intervention.
Study Overview
Status
Suspended
Conditions
Intervention / Treatment
Detailed Description
The purpose of this study is to determine if a physical activity telehealth intervention will increase the amount of moderate-to-vigorous physical activity among 14-17 year olds who are receiving obesity treatment.
A secondary purpose is to determine if a telehealth physical activity intervention will impact the adolescents' body mass index (BMI) z-score who are receiving treatment for obesity.
The participants will complete questionnaires to measure current physical activity levels, physical activity enjoyment, motivation, and strategies to be active.
The study investigators will also review the participants medical records to get BMI.
Participants will be randomized into either an intervention or standard care control group at a 1:1 ratio (intervention-control).
A computer-generated randomization list will be created by an individual not associated with the study.
The intervention will last 11 weeks, and participants in the intervention group receive standard medical care and will have individual weekly web-meeting using a video conferencing platform, Microsoft Teams.
The weekly meeting is expected to last approximately 30 minutes.
During this meeting, participants will report on the past week's physical activity goals, failures and successes, set goals for the next week, discuss that week's behavioral strategy to promote physical activity for that week, and engage around 5 minutes of physical activity.
The topics that will be discussed in the newsletters and weekly meetings will include behavioral strategies for physical activity changes.
Those in the control group will also receive standard medical care and be contacted weekly for 11 weeks and will be asked about their physical activity levels for the past week.
These meetings will also occur using video conferencing and last 5 minutes.
After a regular visit to the medical clinic (6 weeks from the 1st study visit) the study investigators will review medical records from all participants for height, weight, and BMI.
About 12 weeks after the 1st study visit, during a regular clinic visit all participants will complete questionnaires to measure current physical activity levels, physical activity enjoyment, motivation, and strategies to be active.
The study investigators will also review the participants medical records to get height, weight and BMI.
Study Type
Interventional
Enrollment (Estimated)
24
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Carolina
-
Greenville, North Carolina, United States, 27858
- East Carolina University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 17 years (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- 14-17 years of age
- receiving treatment for obesity
- have a smart device for video conferencing
Exclusion Criteria:
- under 14 years of age
- Pregnant
- Type 1 or Type 2 Diabetes
- Neuromuscular disease that impacts moving
- Parent or child unable to speak or write in English.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Physical Activity
The intervention will last 11 weeks, and participants in the intervention group will have individual weekly web-meeting using a video conferencing platform.
The weekly meeting is expected to last approximately 30 minutes.
During this meeting, participants will report on the past week's physical activity goals, failures and successes, set goals for the next week, discuss that week's behavioral strategy to promote physical activity for that week, and engage around 5 minutes of physical activity.
The topics that will be discussed in the newsletters and weekly meetings will include behavioral strategies for physical activity changes.
Those in the control group will also be contacted weekly for 11 weeks and will be asked about their physical activity levels for the past week.
These meetings will also occur using video conferencing and last 5 minutes.
|
the participants will be encouraged to set their own physical activity goals weekly and using behavioral strategies work towards meeting those goals.
The behavioral strategies will be discussed weekly for 30 minutes a telehealth method.
|
|
No Intervention: Control
During the 11 weeks the participants in the control group will have a weekly check in meeting using a video conferencing platform.
The weekly meeting is expected to last approximately 5 minutes.
During this meeting, participants will report on the past week's physical activity levels.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in physical activity participation
Time Frame: weeks 1 and 12
|
minutes spent in physical activity
|
weeks 1 and 12
|
|
Change in BMI z-score
Time Frame: weeks 1, 6, and 12
|
BMI z-score will be calculated from BMI and CDC normative data
|
weeks 1, 6, and 12
|
|
Change in BMI percentile
Time Frame: weeks 1, 6, and 12
|
BMI percentile will be calculated from BMI and CDC normative data
|
weeks 1, 6, and 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in physical activity enjoyment
Time Frame: weeks 1 and 12
|
physical activity enjoyment scale - Likert rating from 1-5 a higher total summary score means more enjoyment
|
weeks 1 and 12
|
|
Change in physical activity motivation
Time Frame: weeks 1 and 12
|
motivation to exercise scale, Likert scale 1-5 where 1=not very true for me to 5=very true for me; 5 different subscales are calculated: amotivation, external regulation, introjected regulation, identified regulation, and intrinsic motivation
|
weeks 1 and 12
|
|
Change in physical activity strategies
Time Frame: weeks 1 and 12
|
physical activity self management questionnaire, Likert scale 1-5 where 1=not very often to 5=very often.
A higher score means that the person uses more posititve self management strategies to engage in physical activity
|
weeks 1 and 12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Katrina D DuBose, PhD, East Carolina University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 24, 2021
Primary Completion (Actual)
February 15, 2022
Study Completion (Estimated)
December 31, 2025
Study Registration Dates
First Submitted
October 26, 2021
First Submitted That Met QC Criteria
November 5, 2021
First Posted (Actual)
November 17, 2021
Study Record Updates
Last Update Posted (Actual)
June 9, 2023
Last Update Submitted That Met QC Criteria
June 6, 2023
Last Verified
June 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21-001684
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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