A Trial of Two Family-based Childhood Obesity Treatment Programs
A Randomized-controlled Trial to Compare the Reach, Effectiveness and Maintenance of Two Family-based Childhood Obesity Treatment Programs in a Medically Underserved Region
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Jamie M Zoellner, PhD, RD
- Phone Number: 434-962-4488
- Email: jz9q@virginia.edu
Study Contact Backup
- Name: Paul A Estabrooks, PhD
- Phone Number: 402.559.4325
- Email: Paul.estabrooks@unmc.edu
Study Locations
-
-
Virginia
-
Charlottesville, Virginia, United States, 22908-0717
- University of Virginia
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Parent/child dyads will be eligible for participation if they reside in the Dan River Region
- English speaking
child with a BMI percentile ranking of 85 or higher
- Cohort 3 age eligibility changed from 8-12 to 5-15
Exclusion Criteria:
- children with a major cognitive impairment and parents or children with a medical contraindication for moderate physical activity.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: iChoose
12 bi-weekly sessions & 24 IVR calls/12 months, 24 physical activity sessions over 6 months; delivers intervention to parents and children only
|
12 bi-weekly sessions & 24 IVR calls/12 months, 24 physical activity sessions over 6 months; delivers intervention to parents and children only
|
|
Experimental: Family Connections
2 in-person sessions spaced one week apart & 10 IVR calls/6 months, promotes physical activity but does not include structured exercise sessions; delivers intervention to parents only
|
2 in-person sessions spaced one week apart & 10 IVR calls/6 months, promotes physical activity but does not include structured exercise sessions; delivers intervention to parents only
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change From Baseline in Child Body Mass Index (BMI) Z-score at 6 Months
Time Frame: Baseline and 6-months
|
child BMI is converted to a BMI Z score which uses a standardized distribution.
A BMI z score of 0 indicates an average BMI for the childs height, weight, age, and gender.
Positive z-scores indicate the number of standard deviations above the norm, while negative numbers indicate the number of standard deviations below the norm.
Higher z scores indicate a greater BMI status for the child.
The primary outcome is a change score, or the difference between the 6 month BMI z-score and the Baseline BMI z-score.
A negative score will indicate BMI z score status reductions and is a positive finding.
|
Baseline and 6-months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change From Baseline of Parent Body Mass Index (BMI) at 6 Months
Time Frame: Baseline and 6-months
|
BMI is the persons weight divided by the square of their height.
BMI categories help to classify individuals as underweight (less than 18.5), normal (18.5-24.9),
overweight (25-29.9),
and obese (30 or higher).
Parent BMI change scores are the difference between the 6 month calculated BMI and the Baseline BMI.
Negative scores indicate improvement in BMI status over this 6 month period.
|
Baseline and 6-months
|
|
Change From Baseline in the Pediatric Quality of Life Inventory for Children Score at 6 Months
Time Frame: Baseline and 6-months
|
The Pediatric Quality of Life Inventory is a 23-item instruments that assesses four domains of health (physical, emotional, social, and school functioning).
Scoring is reported as a percent (0-100), higher scores indicate better health related quality of life.
The change score is calculated as the difference between the 6 month and baseline scores.
A positive difference is considered an improvement in quality of life.
|
Baseline and 6-months
|
|
Change From Baseline in the Healthy Days Core Module for Parents at 6 Months
Time Frame: Baseline and 6-months
|
The Healthy Days Core Module is a measure of quality of life through self reports of the total number of physical and mental health "sick days" (e.g., unable to do daily activities) in the past month.
Higher scores indicate more unhealthy days, or lower quality of life.
Change scores are calculated as the difference between 6 month and baseline scores.
A negative change score indicates a decrease in unhealthy days and thereby and increase in quality of life.
|
Baseline and 6-months
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 19748
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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