Clinical Trials Directory

Trials / Completed

CompletedNCT00359957

Efficacy of Increasing Physical Activity to Reduce Children's Visceral Fat

Activity, Diet, and Visceral Adiposity: New Care Emerging (ADVANCE) Project

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
29 (actual)
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · NIH
Sex
All
Age
7 Years – 12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this trial is to examine whether adding greater physical activity to standard family-based behavioral pediatric obesity treatment decreases the amount of visceral fat among treated overweight children.

Detailed description

Adult studies suggest that greater visceral fat confers more health risk than peripheral fat accumulation and that physical activity interventions (as part of general weight control interventions) are efficacious in reducing adults' visceral fat. There are few studies examining the impact of physical activity and/or general weight loss on children's visceral fat accumulation. The present study compares standard family-based behavioral weight control treatment for pediatric obesity (STANDARD) with standard treatment plus added emphasis on participants attaining high levels of physical activity (ADDED). Both conditions receive the same behavioral dietary intervention and therapeutic contact and attention. The ADDED condition receives the recommendation and goal to be active at least 90 minutes per day, with behavioral strategies targeting increasing and sustaining these high levels of physical activity.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPediatric Obesity Intervention (STANDARD)14 weekly behavioral intervention visits with parent and child; individual family sessions (25-30 minutes) and separate parent and child groups (40 minutes)
BEHAVIORALPediatric Obesity Intervention + High Activity (ADDED)14 weekly behavioral intervention visits with parent and child; individual family sessions (25-30 minutes) and separate parent and child groups (40 minutes)

Timeline

Start date
2006-07-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2006-08-03
Last updated
2010-03-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00359957. Inclusion in this directory is not an endorsement.