A Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity
Primary Purpose
Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Nutritional Counseling
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring Obesity, Nutritional counseling, Physical activity, Food diary
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.
Sites / Locations
- Albert Einstein College of Medicine West Campus CRC
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Group nutritional counseling
Individual nutritional counseling
Arm Description
In this arm, the Nutritionist will conduct the nutritional counseling with numerous patient families as a group
In this arm the nutritionist conducts the nutritional counseling with one patient family at a time
Outcomes
Primary Outcome Measures
Change I Mean Body Mass Index
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 Outcome Measures
Change in BMI with diet
The secondary aim of the study is to determine if the change in BMI is associated with changes in the dietary composition. All the secondary outcomes will be measured by Pearson correlation coefficients or multi-variable linear regression models as appropriate to calculate this.
Change in BMI with physical activity
The study will assess if there is a change in BMI with increased physical activity
Change in BMI with metabolic profile
Study will assess if the change in BMI affects Metabolic profile of the subject.
Full Information
NCT ID
NCT01840631
First Posted
March 8, 2013
Last Updated
October 10, 2018
Sponsor
Albert Einstein College of Medicine
1. Study Identification
Unique Protocol Identification Number
NCT01840631
Brief Title
A Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity
Official Title
A Randomized Controlled Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity
Study Type
Interventional
2. Study Status
Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
April 2013 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
June 1, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Albert Einstein College of Medicine
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Obesity, Nutritional counseling, Physical activity, Food diary
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group nutritional counseling
Arm Type
Active Comparator
Arm Description
In this arm, the Nutritionist will conduct the nutritional counseling with numerous patient families as a group
Arm Title
Individual nutritional counseling
Arm Type
Active Comparator
Arm Description
In this arm the nutritionist conducts the nutritional counseling with one patient family at a time
Intervention Type
Behavioral
Intervention Name(s)
Nutritional Counseling
Intervention Description
Participants enrolled will be randomized into group nutrition counseling or individual nutrition counseling classes, for a total of 6 classes. Classes will meet one time a month. Classes will cover topics including nutrition, exercise, and behavior to promote healthy eating.
Primary Outcome Measure Information:
Title
Change I Mean Body Mass Index
Description
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.
Time Frame
Baseline, month 6
Secondary Outcome Measure Information:
Title
Change in BMI with diet
Description
The secondary aim of the study is to determine if the change in BMI is associated with changes in the dietary composition. All the secondary outcomes will be measured by Pearson correlation coefficients or multi-variable linear regression models as appropriate to calculate this.
Time Frame
Baseline, month 6
Title
Change in BMI with physical activity
Description
The study will assess if there is a change in BMI with increased physical activity
Time Frame
Baseline, month 6
Title
Change in BMI with metabolic profile
Description
Study will assess if the change in BMI affects Metabolic profile of the subject.
Time Frame
Baseline, month 6
10. Eligibility
Sex
All
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa Underland, MD
Organizational Affiliation
Albert Einstein College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Albert Einstein College of Medicine West Campus CRC
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
12. IPD Sharing Statement
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A Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity
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