N/A
Completed N=90
Translating Habituation Research to Interventions for Pediatric Obesity
Pediatric Obesity · Habituation
Source: ClinicalTrials.gov NCT01208870 ↗
Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Oct 2017
Primary outcomePrimary: Change of Child Body Composition — -16.1; -13.3 percentage of weight
Summary
The purpose of this center grant is to translate basic behavioral science on habituation theory into clinical intervention using a vertical hierarchical approach from laboratory studies to field studies to the clinical intervention to improve weight loss outcomes in pediatric obesity treatment.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change of Child Body Composition |
-16.1; -13.3 | — |
| PRIMARY Change Parent Body Composition |
-3.6; -3.1 | — |
| SECONDARY Change in Dietary Intake of Calories |
-716.5; -730.6; -916.0; -962.2; -432.4; -230.3 | — |
| SECONDARY Change in Parent Delay Discounting |
0.003; 0.032; -0.005; 0.020; -0.003; 0.024 | — |
| SECONDARY Change in Child Delay Discounting |
0.017; 0.006; 0.030; 0.025; 0.038; 0.021 | — |
| SECONDARY Changes in Variety Measures |
-12.5; -16.7; -6.3; -11.3; -0.0; -8.0 | — |
Eligibility Criteria
Inclusion Criteria
- Children ages 8-12 years of age
- At or above 85th BMI percentile
- Children must eat almost all meals with the exception of school lunch with the family.
- Overweight parent
Exclusion Criteria
- Children who do not like the study foods, who are allergic to the study foods or who are on special diets and cannot consume the study foods.
- Families with children with a co-morbid psychiatric diagnosis or parents who are depressed, have schizophrenia, substance abuse or a history of eating disorders.
- The parent and child must not have any physical restrictions that would preclude them from making the requisite behavioral changes.
- Children must be able to read at a 3rd grade reading level and must be able to demonstrate the ability to keep dietary and activity records in a stimulated interview.
Data sourced from ClinicalTrials.gov (NCT01208870). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.