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Kansas City, Kansas 66160


Purpose:

The goal of this study is to explore the impact of two different diets (conventional vs. enhanced stop light) and two different delivery systems (face-to-face vs. remote) on weight across 18 months in overweight and obese adolescents with intellectual and developmental disabilities.


Study summary:

Rates of obesity and obesity related chronic health conditions are higher in adolescents with Intellectual and Developmental Disabilities (IDD) than those in the general population. Many of the negative health consequences observed in obese adults are already present in obese adolescents with IDD. This study is a 3 group randomized trial to evaluate the intervention delivery system and type of reduced energy diet. The investigators will randomize 123 overweight/obese adolescents with mild to moderate IDD to one of 3 groups for an 18 month trial (6 month weight loss; 12 month weight maintenance): group 1) Face-To-Face/CD group 2) Technology delivery/CD group 3) Technology delivery/eSLD. All participants will receive a progressive program of physical activity. Participants on the CD diet will be asked to consume a nutritionally balanced, reduced energy, high volume, lower fat ( fat=20-30% energy) diet. Participants on the eSLD will consume pre-packaged portion controlled meals with the addition of 5 fruits and vegetables per day. FTF will meet with a health educator and will track progress using pen and paper records for both physical activity and diet. TECH groups will receive the intervention using an iPad with the FaceTimeTM application for video meetings with a health educator and will track progress using the Lose it! application for both physical activity and diet.


Criteria:

Inclusion Criteria: - Age 13-21 yrs - Mild (IQ of 74-50) or moderate (IQ 40-49) IDD, - Of sufficient functional ability to understand directions, communicate preferences (e.g. foods), wants (e.g. more to eat/drink), and needs (e.g. assistance with food preparation) through spoken language. - Overweight or obese (BMI ≥ 85th%ile on CDC growth charts, or waist circumference to height ratio > 0.5 - Living at home with a parent or guardian. - Internet access in the home. - No plans to relocate outside the study area over the next 18 mos - Physician consent for PA and diet. Exclusion Criteria: - Insulin dependent diabetes - Participation in a weight management program involving diet and PA in the past 6 mos - Eating disorders, serious food allergies, consuming special diets, aversion to common foods, - Diagnosis of Prader-Willi Syndrome - Currently pregnant, planning on/becoming pregnant during the study. - Unable to participate in moderate to vigorous PA.


NCT ID:

NCT02561754


Primary Contact:

Principal Investigator
Joseph E Donnelly, EdD
University of Kansas Medical Center


Backup Contact:

N/A


Location Contact:

Kansas City, Kansas 66160
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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