- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01546727
Behavioral Treatment for Obese Preschoolers (LAUNCH)
December 27, 2016 updated by: Children's Hospital Medical Center, Cincinnati
Clinic and Home Family Based Behavioral Treatment for Obese Preschoolers
This study is a 3 arm, randomized, parallel group randomized clinical trial to test a clinic and home family behavioral intervention (LAUNCH) against 1) motivational interviewing (attention control; MI) and 2) standard of care (true standard of care control; STC) with 168 children ages 2 to 5 years who meet the criteria for obesity (>95th percentile for body mass index; BMI).
Participants will be randomized to receive a 6 month intervention (LAUNCH, MI) or standard of care.
The primary end-point will be change in BMI z-score at the end of treatment.
The investigators will also assess maintenance of treatment gains at 6 and 12 months after treatment, and changes in factors thought to be mechanisms for change in weight (food intake and activity level), changes in the obesiogenic environment (parent weight, food intake and activity, and changes in the home food environment) and factors that could be negatively impacted (parent and child eating and feeding interactions).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Obesity now affects an estimated 2.8 million children between the ages of 2 and 5 years, as the prevalence of obesity among preschool school age children has almost tripled from 5% of the population in 1971-1980 to 13.9% by 2004.
Being obese at age 5 confers a 47 times greater risk of being overweight or obese at age 12.
In fact being obese any time between 2 and 5 year increases the risk of remaining overweight or obese as an adult by four times the risk of nonobese preschoolers.
Being obese as a preschooler also increases the risk of a number of serious health conditions, including a 2.6 times greater risk of developing type 2 diabetes by age 21 years.
In fact, the obesity rate among preschoolers is thought to impose such a cumulative health risk across the life span that children born today, for the first time in history, are expected to have a shorter life expectancy than their parents by to 2 to 5 years.
Early effective treatments for establish obesity during the preschool years have the potential to change the trajectory of obesity and related co-morbid health condition across the life-span by reducing obesity and changing the development of lifestyle habits of diet and exercise at a time when these are being formed.
Yet research on interventions to reduce obesity in preschool children is severely limited and none exist that addresses established obesity in this age group.
Therefore the current study has the potential to have a significant impact on public health by providing evidence-based treatment for obesity in preschoolers, a developmental period in which eating and activity patterns are being formed, that could significantly impact the trajectory of obesity thereby decreasing the population obesity rates and associated healthcare costs at across the life span.
Fortunately, investigators are on their way to addressing the problem of obesity reduction in already obese preschoolers.
The investigators have developed and conducted a pilot randomized clinical trial of a treatment program aimed at reducing obesity in already obese preschool children.
The program (Learning about Activity and Understanding Nutrition for Child Health: LAUNCH) is tailored to the developmental stage of preschool children and produced promising preliminary results.
In the proposed trial a 3 arm, randomized, parallel group design will test LAUNCH against 1) motivational interviewing (attention control; MI) and 2) standard of care (true standard of care control; STC) with 168 children ages 2 to 5 years who meet the criteria for obesity (>95th percentile for body mass index; BMI).
Participants will be randomized to receive a 6 month intervention (LAUNCH, MI) or standard of care.
The primary end-point will be change in BMI z-score at the end of treatment.
The investigators will also assess maintenance of treatment gains at 6 and 12 months after treatment, and changes in factors thought to be mechanisms for change in weight (food intake and activity level), changes in the obesiogenic environment (parent weight, food intake and activity, and changes in the home food environment) and factors that could be negatively impacted (parent and child eating and feeding interactions).
Study Type
Interventional
Enrollment (Actual)
167
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ohio
-
Cincinnati, Ohio, United States, 45229
- Cincinnati Children's Hospital Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
2 years to 5 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Children ages 2 years 0 months to 5 years 11 months
- BMI percentile at or above the 95th percentile for age- and gender, but no more than 100% above the median BMI for age and gender.
- English-speaking
- Live within 50 miles of Cincinnati Children's Hospital Medical Center (CCHMC)
- Medical clearance from the child's pediatrician to participate.
Exclusion Criteria:
- Medical conditions known to promote obesity (e.g., Prader-Willi syndrome, Cushing's syndrome)
- Already involved with another weight control program
- Taking weight-affecting medications (e.g., steroids).
- A disability or illness that would preclude them from engaging in at least moderate intensity physical activity
- Developmental disability
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Family Behavioral Treatment
This intervention will provide nutritional counseling for a health diet, parent training in effective child behavioral management strategies, and stimulus control of the home environment delivered via group based clinic visits and individual home visits on alternate weeks
|
Three months of weekly treatment delivered via alternating group based clinic visits and individual home visits followed by three months of every other week treatment alternating between clinic and home.
Other Names:
|
|
Active Comparator: Motivational Interviewing
This intervention will shared information with parents about their child's weight and use motivational interviewing to elicit changes parents would like to make to their child diet and activity patterns.
|
Motivational interviewing will be delivered at the same frequency at the behavioral intervention with 4 in-person visits spaced at the first visit, month 3 and month 5. Phone calls will be conducted weekly during the first 3 months and every other week during months 4 through 6.
Other Names:
|
|
No Intervention: Standard of Care
Participants in this arm will be followed over time and be assessed on the primary and secondary outcomes at the same time points as the two treatment arms
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in BMIz score
Time Frame: Baseline to 6 months
|
Body Mass Index z-score
|
Baseline to 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in BMI z at follow up
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Baseline, 6 months, 12 months, 18 months
|
|
|
Change in Caloric Intake
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Three 24 hour dietary recalls at each time point
|
Baseline, 6 months, 12 months, 18 months
|
|
Change in Physical Activity
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Physical Activity will be measured using Accelermeters set in 15 sec epochs
|
Baseline, 6 months, 12 months, 18 months
|
|
Change in home health environment
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Home observation recording of food (e.g.,fruits, vegetables, high calorie foods and beverages)and presence of TV in child's bedroom
|
Baseline, 6 months, 12 months, 18 months
|
|
Changes in parent calorie intake
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Will assess using Block 2005 Food Frequency
|
Baseline, 6 months, 12 months, 18 months
|
|
Changes in parent physical activity
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Will be assessed using the Paffenbarger Activity Questionnaire for calorie expenditure
|
Baseline, 6 months, 12 months, 18 months
|
|
Parenting and Child Eating Behaviors
Time Frame: Baseline, 6 month, 12 months, 18 months
|
Will assess using Parenting Styles and Dimensions, About Your Child's Eating - Revised, and Child Feeding Questionnaire
|
Baseline, 6 month, 12 months, 18 months
|
|
Change in Health Related Quality of Life
Time Frame: Baseline, 6 months, 12 months, 18 months
|
Will be assessed using the PedQL
|
Baseline, 6 months, 12 months, 18 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Lori J Stark, Ph.D., Children's Hospital Medical Center, Cincinnati
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Stark LJ, Filigno SS, Kichler JC, Bolling C, Ratcliff MB, Robson SM, Simon SL, McCullough MB, Clifford LM, Stough CO, Zion C, Mara CA. Maintenance Following a Randomized Trial of a Clinic and Home-based Behavioral Intervention of Obesity in Preschoolers. J Pediatr. 2019 Oct;213:128-136.e3. doi: 10.1016/j.jpeds.2019.05.004. Epub 2019 Jun 21.
- Robson SM, Ziegler ML, McCullough MB, Stough CO, Zion C, Simon SL, Ittenbach RF, Stark LJ. Changes in diet quality and home food environment in preschool children following weight management. Int J Behav Nutr Phys Act. 2019 Feb 4;16(1):16. doi: 10.1186/s12966-019-0777-6.
- Stark LJ, Spear Filigno S, Bolling C, Ratcliff MB, Kichler JC, Robson SM, Simon SL, McCullough MB, Clifford LM, Odar Stough C, Zion C, Ittenbach RF. Clinic and Home-Based Behavioral Intervention for Obesity in Preschoolers: A Randomized Trial. J Pediatr. 2018 Jan;192:115-121.e1. doi: 10.1016/j.jpeds.2017.09.063. Epub 2017 Nov 14.
- Stark LJ, Filigno SS, Bolling C, Ratcliff MB, Kichler JC, Robson SL, Simon SL, McCullough MB, Clifford LM, Stough CO, Zion C, Ittenbach RF. Learning about Activity and Understanding Nutrition for Child Health (LAUNCH): Rationale, design, and implementation of a randomized clinical trial of a family-based pediatric weight management program for preschoolers. Contemp Clin Trials. 2017 Jan;52:10-19. doi: 10.1016/j.cct.2016.10.007. Epub 2016 Oct 21.
- Robson SM, Bolling C, McCullough MB, Stough CO, Stark LJ. A Preschool Obesity Treatment Clinical Trial: Reasons Primary Care Providers Declined Referrals. J Pediatr. 2016 Oct;177:262-266.e1. doi: 10.1016/j.jpeds.2016.06.027. Epub 2016 Jul 22.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2012
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
December 1, 2016
Study Registration Dates
First Submitted
March 2, 2012
First Submitted That Met QC Criteria
March 6, 2012
First Posted (Estimate)
March 7, 2012
Study Record Updates
Last Update Posted (Estimate)
December 28, 2016
Last Update Submitted That Met QC Criteria
December 27, 2016
Last Verified
December 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01DK091251 (U.S. NIH Grant/Contract)
- 1R01DK091251-01A1 (U.S. NIH Grant/Contract)
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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