For the Health of Our Children--Clinic Based Treatment of Childhood Obesity
Primary Purpose
Obesity
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Behavioral counseling
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring Childhood obesity treatment, Motivational interviewing
Eligibility Criteria
Inclusion Criteria:
- any patient at the participating clinic between the ages of 4-8 years who have a BMI ≥ the 85th percentile
Exclusion Criteria:
- emergent health concern
- serious chronic health concern or recent gastrointestinal illness which may have resulted in weight loss
- on medications known to affect weight
Sites / Locations
- Fairview Children's Clinic
- University of Minnesota
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
behavioral counseling
Instructions in school readiness and performance
Arm Description
Receive counseling via motivational interviewing seeking to encourage health eating habits and increased physical activity
Parents receive instructions in school readiness and performance
Outcomes
Primary Outcome Measures
Body Mass Index Z-score Change
Change in body mass index z-score change over the three month time period
Secondary Outcome Measures
Sugar Sweetened Beverages
Change in reported intake of sugar sweetened beverages
Full Information
NCT ID
NCT01625910
First Posted
April 10, 2012
Last Updated
January 26, 2017
Sponsor
University of Minnesota
1. Study Identification
Unique Protocol Identification Number
NCT01625910
Brief Title
For the Health of Our Children--Clinic Based Treatment of Childhood Obesity
Official Title
For the Health of Our Children--Clinic Based Treatment of Childhood Obesity: The Feasibility of Recruitment and the Effectiveness of a Low-intensity Stage
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Childhood obesity is a major public health problem in the U.S. Currently approximately one in three children is considered overweight or obese. Most overweight children grow to become overweight adults. It is unclear how effective pediatricians and other primary care physicians can be in assisting overweight children to normalize their body weight. Expert guidelines have been established, but are currently untested.
This study will randomize overweight and obese children between the ages of 4 and 8 years old to either the recommended treatment guidelines or a control (non-intervention) group.
The purpose of this study is to evaluate the ability (a) to recruit overweight children between the ages of 4 and 8 years old (b) to remeasure the children three months after enrollment and (c) to reduce childhood obesity via implementation of the recommended treatment guidelines.
Detailed Description
3. Research Plan:
a. Specific Aims and Hypothesis: In 2007, an expert committee, composed of representatives from 16 major clinical organizations (including the PI of this proposal), published recommendations for primary care office-based treatment of childhood obesity. Seeking both clinical and cost-effectiveness, the recommendations call for staged treatment that starts with low intensity, and then, if unsuccessful, increases to a higher frequency of visits. The committee acknowledged that this staged approach "has not been evaluated." Recent reviews conclude that treatment of childhood obesity can be efficacious. However, most studies were conducted in highly controlled tertiary care research settings and involved a large number of direct contact hours (e.g. many with ≥ 35 contact hours). Research evaluating the translation of these encouraging findings into more real-world clinical settings has been lacking. Specifically, there is little research assessing (1) the feasibility of recruitment from primary care clinics or (2) whether low intensity treatment (i.e. the initial phase of the staged approach recommended by the expert committee) has any benefit on weight loss.
Aim #1: To assess the feasibility of recruiting overweight and obese children, ages 4-8 years, from a large, urban pediatric primary care clinic, randomizing them to either low-intensity treatment or a control group, and then re-measuring them at approximately 3-months from the date of recruitment.
o Our hypothesis is that we will be able to recruit approximately 70 parent/child dyads and re-measure 80% at 3-months.
Aim #2: To evaluate whether the proportion of children who decrease their BMI z-score over a 3-month period is higher in those randomly assigned to the intervention group compared with those in the control group.
Our hypothesis is that the intervention will result in a larger proportion of children decreasing BMI z-score over a 3-month period.
Results from Aims 1 and 2 will be used to plan for an NIH proposal. If the low intensity treatment of this proposal shows a trend toward improvement over usual care, this will justify a full scale, R01 trial testing the complete recommendations of the expert committee. If few subjects in the intervention group have decreasing BMI z-scores, then a smaller NIH trial would be needed to test an amended low-intensity treatment stage with more parent/child contact (e.g. emails, home visits, phone calls).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Childhood obesity treatment, Motivational interviewing
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
72 (Actual)
8. Arms, Groups, and Interventions
Arm Title
behavioral counseling
Arm Type
Experimental
Arm Description
Receive counseling via motivational interviewing seeking to encourage health eating habits and increased physical activity
Arm Title
Instructions in school readiness and performance
Arm Type
Placebo Comparator
Arm Description
Parents receive instructions in school readiness and performance
Intervention Type
Behavioral
Intervention Name(s)
Behavioral counseling
Other Intervention Name(s)
Motivational Interviewing, Pediatric obesity treatment
Intervention Description
Counseling of parents to improve their child's diet and physical activity
Primary Outcome Measure Information:
Title
Body Mass Index Z-score Change
Description
Change in body mass index z-score change over the three month time period
Time Frame
Three months
Secondary Outcome Measure Information:
Title
Sugar Sweetened Beverages
Description
Change in reported intake of sugar sweetened beverages
Time Frame
Three months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
any patient at the participating clinic between the ages of 4-8 years who have a BMI ≥ the 85th percentile
Exclusion Criteria:
emergent health concern
serious chronic health concern or recent gastrointestinal illness which may have resulted in weight loss
on medications known to affect weight
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven D Stovitz, MD, MS
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fairview Children's Clinic
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55414
Country
United States
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55414
Country
United States
12. IPD Sharing Statement
Learn more about this trial
For the Health of Our Children--Clinic Based Treatment of Childhood Obesity
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