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Clinical Trials/NCT01840631
NCT01840631
Completed
N/A

A Randomized Controlled Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity

Albert Einstein College of Medicine1 site in 1 country90 target enrollmentApril 2013
ConditionsObesity

Overview

Phase
N/A
Intervention
Not specified
Conditions
Obesity
Sponsor
Albert Einstein College of Medicine
Enrollment
90
Locations
1
Primary Endpoint
Change I Mean Body Mass Index
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Aim 1 - The primary aim of the study is to assess whether group counseling is a non-inferior intervention compared to the usual care of individual counseling in the management of childhood obesity. In order to achieve this aim, the investigators will compare the mean change in BMI after 6 months of intervention in the two study arms.

Aim 2 - The secondary aim of the study is to determine if the change in BMI is associated with changes in the dietary composition, physical activity and metabolic profile.

Detailed Description

This is a non-inferiority study to determine the sample size needed for a larger study to explore an intervention strategy focused on nutrition counseling to maximize weight loss and minimize cardiovascular risk factors in obese children and adolescents. This is a prospective parallel arm, randomized trial, to study the impact of nutritional counseling in an individual vs. group setting. There will be a total of four groups. Obese pre-adolescents (ages 9-12) and adolescents (ages 13-17) will be randomized into two interventions: individual nutrition counseling or group nutrition counseling. Subjects will receive the same information in both interventions. All content will be developed prior to starting the intervention. Each group session will have a maximum of 7 children with 1 parent/caregiver per child and a minimum of 5 children with a caregiver. Group sessions will be one time a month for 60 minutes (30 minutes for dietetic session and 30 minutes for discussion/questions) and individual sessions will be one time a month for 30 minutes. There will be 6 sessions for each group. All groups will receive standard of care for physical fitness counseling which includes recommending 1 hour of physical activity a day and limiting screen time to less than 2 hours a day. All groups will be evaluated for depression and appropriately referred if found to be depressed. Behavioral strategies, like mindful eating, will be included in the nutrition education.

Registry
clinicaltrials.gov
Start Date
April 2013
End Date
June 1, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lisa Underland

Asst. Professor, Pediatrics

Albert Einstein College of Medicine

Eligibility Criteria

Inclusion Criteria

  • Subjects 9-17 years of age with a BMI percentile for age of ≥95
  • Subjects must be able to attend monthly sessions with a parent and/or guardian.

Exclusion Criteria

  • Subjects with diabetes at baseline, mental or psychological disease that would interfere with understanding, disease or medication causing obesity or weight loss, and participants in an alternative weight management program will not be included in the study.
  • Subjects with impaired glucose tolerance will not be excluded from participation.
  • Non-English speaking subjects will not be excluded.

Outcomes

Primary Outcomes

Change I Mean Body Mass Index

Time Frame: Baseline, month 6

The primary aim of the study is to assess whether group counseling is a non-inferior intervention compared to the usual care of individual counseling in the management of childhood obesity. In order to achieve this aim, investigators will compare the mean change in BMI after 6 months of intervention in the two study arms. As per previous studies, it is expected the group intervention arm to achieve a mean BMI reduction of 0.8 +/- 1.4 greater than the control arm. The study also posits that a difference in mean BMI change as low as 0.1 would be clinically equivalent.

Secondary Outcomes

  • Change in BMI with diet(Baseline, month 6)
  • Change in BMI with metabolic profile(Baseline, month 6)
  • Change in BMI with physical activity(Baseline, month 6)

Study Sites (1)

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