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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06148246
Other study ID # IRB202102295
Secondary ID R21HD100743
Status Recruiting
Phase N/A
First received
Last updated
Start date January 18, 2024
Est. completion date December 1, 2024

Study information

Verified date January 2024
Source University of Florida
Contact Danielle E Jake-Schoffman, PhD
Phone (352) 294-1816
Email djakeschoffman@ufl.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall aim of this study is to test the acceptability and usability of a mobile application (app) for family-based physical activity and weight gain prevention among parent/guardian and child (ages 9-12 years) dyads.


Description:

This study includes a 12-week active intervention period, following by a 6-week observational period for a total of 18 weeks. Interested participants will complete a study orientation webinar, then continue to a baseline visit and online questionnaires if interested. They will then complete 7-days of accelerometry monitoring to measure current physical activity levels. If eligible, they will then be randomized to a study group, and attend a brief kick-off meeting to receive their Fitbits and study apps. The intervention period is 12 weeks, all remotely delivered. Both intervention conditions focus on families working to increase their moderate- to-vigorous intensity physical activity. At 12 weeks, families will attend a brief in-person assessment visit and complete online questionnaires and 7 days of accelerometry. There is no active intervention between weeks 13-18. At week 18, families will attend a brief in-person assessment visit and complete online questionnaires and 7 days of accelerometry, as well as complete a semi-structured interview via Zoom to discuss their experiences and provide feedback for future program modifications.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 1, 2024
Est. primary completion date December 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 9 Years to 65 Years
Eligibility Inclusion Criteria: 1. Parent (or legal guardian) must: - Be between 18-65 years old - Use a mobile Apple or Android device (e.g., smartphone, tablet) - Have a mobile data plan or reliable access to home Wi-Fi - Have an active Facebook account 2. Child must: - Be 9-12 years old - Live in the residence of parent (at least 50% of the time) 3. Child and parent must: - Be able to speak and read English. - Be insufficiently physically active (adult: <150 minutes/week moderate physical activity or <75 minutes/week vigorous physical activity, child: <6 days/week of 60 minutes moderate- to vigorous-intensity physical activity) - Be able to engage in physical activity. - Live within 25 miles of the UF campus Exclusion Criteria: 1. Parent currently, or trying to become, pregnant. 2. Current participation in a structured physical activity or weight loss program (children playing sports will be permitted) 3. Currently enrolled in a research study focused on changing diet or physical activity. 4. Use of weight loss medications 5. Child BMI >95th percentile 6. Child current use of Fitbit (or similar physical activity device) 7. History of eating disorder 8. One parent and one child per family unit may enroll

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Family Fit Condition
Dyads in the Family Fit condition will use the Family Fit app and a Fitbit for 18 weeks, working to increase their moderate- to vigorous-intensity physical activity.
Fitbit Only Condition
Dyads in the Fitbit only condition will use a Fitbit and the Fitbit app for 18 weeks, working to increase their moderate- to vigorous-intensity physical activity.

Locations

Country Name City State
United States UF College of Health and Human Performance Gainesville Florida

Sponsors (2)

Lead Sponsor Collaborator
University of Florida Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recruitment Number of dyads screened and enrolled; rate of recruitment Baseline
Primary Use rates Use rates of the Family Fit app summarized from back-end data from the app 12 weeks
Primary Acceptability Satisfaction, perceived appropriateness, intent to continue to use intervention materials, likelihood of recommending the program to a friend, open-ended questions: overall satisfaction with program and suggestions for improvement 12 weeks
Primary Retention Number of dyads per condition who complete follow-up assessments 12 weeks 18 weeks
Secondary Sustainability Use of Family Fit app, Fitbit app, and Fitbit devices from weeks 13-18 12 weeks and 18 weeks
Secondary Usability Scores from System Usability Scale 12 weeks and 18 weeks
Secondary Contamination Use of outside physical activity programs, devices, and apps during the study 12 weeks and 18 weeks
Secondary Average minutes/day of moderate- to vigorous-intensity physical activity, accelerometry Actigraph accelerometers to be used; 7 days of wear time will be requested from participants at each time point Baseline, 12 weeks, 18 weeks
Secondary Average minutes/day of moderate- to vigorous-intensity physical activity, self-report Godin Leisure-Time Exercise Questionnaire Baseline, 12 weeks, 18 weeks
Secondary BMI (parents) Body weight (to the nearest 0.1 lbs), height (to the nearest 0.25 inch) with standard protocols; BMI calculated as kg/m^2 Baseline, 12 weeks, 18 weeks
Secondary BMI percentile (child) Body weight (to the nearest 0.1 lbs), height (to the nearest 0.25 inch) with standard protocols; BMI percentile using standardized charts Baseline, 12 weeks, 18 weeks
Secondary Family cohesion Moos et al. family environment scale Baseline, 12 weeks, 18 weeks
Secondary Social support Kiernan et al. adaptation of social support scale Baseline, 12 weeks, 18 weeks
Secondary Family communication Measure from the National Longitudinal Study of Adolescent Health (Add Health) Baseline, 12 weeks, 18 weeks
Secondary Family engagement Measure from the National Longitudinal Study of Adolescent Health (Add Health) Baseline, 12 weeks, 18 weeks
Secondary Family closeness Measure from the National Longitudinal Study of Adolescent Health (Add Health) Baseline, 12 weeks, 18 weeks
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