Summary

Eligibility
for people ages 7-12 (full criteria)
Healthy Volunteers
healthy people welcome
Location
at La Jolla, California
Dates
study started
estimated completion
Principal Investigator
by Kay Rhee

Description

Summary

The purpose of this application is to evaluate whether a pediatric weight control program that incorporates comprehensive parenting training with behavioral therapy can increase weight loss in children compared to traditional family-based behavioral therapy programs. Since certain parenting styles are associated with greater weight loss during interventions and appear to enhance the impact of key behavioral strategies, adding parenting training to these interventions may increase the overall effectiveness of these programs and increase our ability to help children obtain a healthy weight. This project could result in identifying an improved method of pediatric obesity treatment that provides additional benefits to the growth and development of children via improved self-regulatory behaviors.

Official Title

Parent Training Program to Improve Outcomes in Childhood Obesity Treatment

Details

Authoritative parenting style has been associated with decreased obesity risk in children, increased weight loss during interventions, and can modify the delivery and impact of weight control strategies, making them more effective. At this time, gold-standard treatment for childhood obesity is family-based behavioral therapy (FBT). This treatment relies on behavioral strategies and the use of praise and a positive reinforcement system to change eating and activity behaviors, but does not target other aspects of parenting. Broadening parenting instruction to include effective limit-setting behaviors, parent-child communication, and authoritative parenting may increase parents' confidence and ability to successfully make behavior changes and modify the impact of the behavioral strategies being used. In this application, the investigators propose to test the efficacy of a 20-week weight control program that combines traditional family-based behavioral therapy with comprehensive parenting training (FBT-PT) and compare it to traditional family-based behavioral therapy (FBT). The investigators hypothesize that there will be an additive effect of parenting training such that FBT-PT will have a greater effect on child weight loss (measured by BMI z-score) than traditional FBT. In addition, the investigators will measure parenting style, parenting strategies, behavioral strategies, and child factors (like impulsive behavior and temperament) to better understand the mediators and moderators of weight loss. These measures will be obtained by standard self-report measures and videotape encounters, allowing one to more objectively measure parenting dimensions. Clinical outcomes, like drop-out and acceptability, will also be assessed from the two treatment arms. The purpose of this study is to evaluate the effect of adding a comprehensive parenting training to traditional FBT. If successful, this program will be able to increase our ability to help children successfully lose weight.

Keywords

Pediatric Obesity, Obesity treatment, Parenting training, Parenting style, Family-based behavioral therapy, Obesity, Family-based behavioral therapy (FBT), Parenting training and FBT

Eligibility

You can join if…

Open to people ages 7-12

  1. Children between the ages of 7 and 12 years old;
  2. BMI ≥85th percentile but <100% overweight, so as to limit those children who are morbidly obese and are in need of more intense medical treatment;
  3. Children with mothers who are willing to attend 20 weekly group sessions and be randomized to either treatment arm;
  4. Have at least one parent who is overweight or obese (BMI≥25); and
  5. Parents who speak English at a 5th grade level.

You CAN'T join if...

  1. Children with serious medical conditions that affect their weight;
  2. Children taking medication that affect appetite or weight;
  3. Children with severe developmental delay or disability that would affect participation;
  4. Children or parents with psychological illness that would limit treatment participation;
  5. Families who will move out of the area within the time frame of the study.

Location

  • University of California, San Diego
    La Jolla California 92093 United States

Lead Scientist at UCSD

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, San Diego
ID
NCT02976636
Study Type
Interventional
Participants
Expecting 160 study participants
Last Updated