- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06546696
The ADAPT Trial: Adapting Evidence-Based Obesity Interventions in Community Settings
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In Aim 1, the investigators will conduct a community readiness assessment for COACH in 50 community centers serving rural, minority, and low-income families in middle TN. In 25 randomly selected community centers, the investigators will use a systematic process to adapt the intervention protocol based on the assessment results, while maintaining fidelity to COACH's core components. In Aim 2, in a cluster-randomized trial, the investigators will test the comparative effectiveness of each implementation strategy (adaptation vs. original program) on the implementation outcomes of reach, adoption, implementation, and maintenance. In Aim 3, the investigators will test the comparative effectiveness of the adapted and original intervention.
This research is innovative because it uses adaptation science as a potential solution to reduce health disparities in childhood obesity. By testing this intervention in a community resource available to 230 million Americans (community centers), the investigators aim to create a scalable obesity intervention that could be implemented in traditionally underserved populations across the country. This study will also develop and test a theory-based process for adapting behavioral interventions for both obesity and other health outcomes among diverse rural and urban communities.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: William J Heerman, MD, MPH
- Phone Number: 615-322-7080
- Email: Bill.Heerman@vumc.org
Study Contact Backup
- Name: Laura Adams, RD, MBA
- Phone Number: 615-875-7298
- Email: Laura.E.Adams@vumc.org
Study Locations
-
-
Tennessee
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Nashville, Tennessee, United States, 37212
- Recruiting
- Vanderbilt University Medical Center
-
Contact:
- William J Heerman, MD, MPH
- Phone Number: 615-322-7080
- Email: Bill.Heerman@vumc.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Child with an age ≥ 6 years and < 12 years
- Child body mass index ≥95th percentile for age and sex on standardized CDC growth curves
- Index parent/legal guardian with an age ≥18 years
- Parent and child speak English or Spanish
- Family resides within or frequently visit selected zip codes within Middle TN surrounding the partnering community centers;
- Have parental commitment to participate in a 6-month study;
- Have the ability to view online trainings
- Complete baseline data collection, including parent and child height and weight and at least 90% of baseline survey items.
Exclusion Criteria:
- Participant child has been diagnosed with Down Syndrome, Autism, or any other developmental disorders that impact metabolism or behaviors that would preclude participation in group physical activity settings;
- Either the participant caregiver or child is unable to participate in light to moderate physical activity;
- Participant caregiver has a serious mental or neurologic illness that impairs ability to consent/participate.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: COACH Intervention
COACH intervenes at 3 levels: the individual child, the family, and the community. Child-Level Intervention Content: We will direct skill-building lessons toward the child at developmentally appropriate levels. Family-Level Intervention Content: Curricular components for parents are designed to leverage parents as agents of change for their children. As such, the group-based sessions includes realistic goal setting (SMART goals), strategies to navigate barriers, training in physical activity, and group-based accountability. During the session, parents and children will participate in a low to moderate physical activity. Community-Level Content: The intervention is delivered in the context of a widely available community resource, local community centers across Middle Tennessee. Online Platform: All participants will have access to an online on-demand health behavior change curriculum. Modules are self-paced and will take approximately 7 hours. |
COACH is a multi-level intervention, consisting of 1) developmentally appropriate health curriculum for children; 2) family-based content that both targets parent weight loss and leverages a shared parent-child experience to improve family health behaviors; 3) community-level intervention to improve access and quality of family-based programming at local Parks and Rec centers.
Other Names:
|
|
Active Comparator: Adaptation Arm
The core components of the adaptation arm will mirror the COACH intervention arm.
Each community center will be guided through a process of adapting the specific intervention content, and as such, will be unique to each of the 25 community centers randomized to this arm.
In this way, the study tests the process of adapting the intervention, instead of a specific portfolio of adaptations.
|
COACH is a multi-level intervention, consisting of 1) developmentally appropriate health curriculum for children; 2) family-based content that both targets parent weight loss and leverages a shared parent-child experience to improve family health behaviors; 3) community-level intervention to improve access and quality of family-based programming at local Parks and Rec centers.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Percent of the 95th Body Mass Index Percentile
Time Frame: 6 months post randomization
|
Calculated from CDC growth curves
|
6 months post randomization
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Percent of the 95th Body Mass Index Percentile
Time Frame: 6 weeks post randomization
|
Calculated from CDC growth curves
|
6 weeks post randomization
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Media Use
Time Frame: 6 months post randomization
|
Child Media Use Index
|
6 months post randomization
|
|
Child Sleep
Time Frame: 6 months post randomization
|
Children's Sleep Habits Questionnaire
|
6 months post randomization
|
|
Parent Body Mass Index
Time Frame: 6 weeks post randomization
|
Measured by study staff
|
6 weeks post randomization
|
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Parent Body Mass Index
Time Frame: 6 months post randomization
|
Measured by study staff
|
6 months post randomization
|
|
Child Diet
Time Frame: 6 months post randomization
|
Child Nutrition and Physical Activity Behavior Scale.
Possible range of 0-9 with higher scores indicating healthier diet and physical activity practices.
|
6 months post randomization
|
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Child Physical Activity
Time Frame: 6 months post randomization
|
Child Nutrition and Physical Activity Behavior Scale.
Possible range of 0-9 with higher scores indicating healthier diet and physical activity practices.
|
6 months post randomization
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 241092
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Following the study's conclusion, aggregate data may be made available based on reasonable request.
We will plan to upload a de-identified dataset to the NHLBI BioLINCC database (this upload also includes study protocols).
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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