Treatment of Early Childhood Overweight in Primary Care: Pilot Study

Sponsor
University of Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT01662557
Collaborator
Geisinger Center for Health Research (Other), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
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Study Details

Study Description

Brief Summary

Childhood overweight continues to increase at an alarming rate and the need exists to find effective, accessible intervention strategies to prevent and treat children who are at risk for being overweight or are already overweight. The primary care setting provides an attractive option for families wishing to receive treatment, yet little is known about the feasibility, acceptance or efficacy of this intervention setting. The purpose of this study was to test two different primary care treatments that were intended to increase fruit and vegetable intake, increase physical activity, and reduce sedentary activity in children ages 4-8, who are overweight or at risk for becoming overweight. Both treatments involved the child and a parent/caregiver and both were conducted over a four month period. The parent/child dyads were selected from the pool of families who receive their primary care within the Geisinger Medical Center geographic area and who have been identified by their pediatrician as being overweight or at risk for becoming overweight (BMI >85th percentile for age). One group received weekly mailings which focused on healthy eating, promotion of fruit and vegetable intake and physical activity, and methods to reduce TV viewing time. The second group received a group-based intervention at one of the Geisinger Pediatric Clinic sites using specific behavioral strategies for increasing fruit and vegetable intake, reducing TV viewing and encouraging physical activity. Changes in overweight percentage, child BMI, lipid profile, glucose/insulin levels, and anthropometric measurements were analyzed, as well as treatment satisfaction and acceptance. The investigators hypothesized that children who receive Family Behavior Modification (FBM) in the primary care setting will show greater reductions in Body Mass Index (BMI), BMI z-score, percent overweight and waist circumference, and that children receiving FBM will show greater improvements in dietary intake, increased physical activity, reduced sedentary activity, and improvements in cardiovascular outcomes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Family Behavior Modification
  • Other: Minimal Nutrition Information
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
51 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Treatment of Early Childhood Overweight in Primary Care: Pilot Study
Study Start Date :
Feb 1, 2008
Actual Primary Completion Date :
Mar 1, 2011
Actual Study Completion Date :
Mar 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Family Behavior Modification

Family-based behavior modification with parent and child using goal setting, self monitoring, reinforcement, behavioral skills training, and tasting opportunities.

Behavioral: Family Behavior Modification
5-month intervention for parents and children providing 15 sessions in behavioral skills training in self monitoring, Traffic Light Diet, goal setting, reinforcement and tasting sessions. Of the 15 sessions, 3 were structured as phone sessions.
Other Names:
  • FBM
  • Other: Minimal Nutrition Information

    Weekly mailings emphasizing healthy eating guidelines for families.

    Other: Minimal Nutrition Information
    Families assigned to MNI received a series of 15 mailings on topics related identifying a healthy body weight for children; energy balance and calorie requirements for children; MyPyramid for Kids; portion control; the benefits of physical activity and screen-time reduction; encouraging fruit and vegetable consumption; healthy snacks and smart shopping; and encouraging family meals.
    Other Names:
  • MNI
  • Outcome Measures

    Primary Outcome Measures

    1. Child's Overweight Percentage [Baseline and Month 5]

      Change in child's overweight percentage will be measured from baseline to end of treatment (month 5)

    2. Body Mass Index z-score (BMI-z) [Baseline and Month 5]

      Change in BMI-z score will be measured from baseline to end of treatment (month 5)

    3. Waist Circumference [Baseline and Month 5]

      Change in child's waist circumference will be measured from baseline to end of treatment (month 5).

    4. Body Mass Index (BMI) [Baseline and Month 5]

      Change in BMI will be measured from baseline to end of treatment (month 5).

    Secondary Outcome Measures

    1. Dietary Intake [Baseline and Month 5]

      Change in dietary intake (kcals, protein, fat, saturated fat, cholesterol, fiber, carbohydrate, fruit/veg servings, Vitamins A and C) will be assessed from baseline to end of treatment (month 5) using 24-hour recall interviews.

    2. Activity Level [Baseline to Month 5]

      Physical activity (sedentary, light, moderate and moderate to vigorous) will be assessed via accelerometry between baseline and end of treatment (month 5).

    3. Insulin (uUnits/ml) [Baseline and Month 5]

      Change in fasting insulin will be measured at baseline and end of treatment (month 5).

    4. Glucose (mg/dl) [Baseline and Month 5]

      Change in fasting glucose levels will be measured from baseline to end of treatment (month 5).

    5. Triglycerides (mg/dl) [Baseline and Month 5]

      Change in fasting triglyceride levels will be measured from baseline to end of treatment (month 5).

    6. HDL (mg/dl) [Baseline and Month 5]

      Change in HDL levels will be measured from baseline to end of treatment (month 5).

    7. LDL (mg/dl) [Baseline and Month 5]

      Change in LDL levels will be measured from baseline to end of treatment (month 5).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    4 Years to 8 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 4-8 year old children

    • overweight or obese (BMI≥85th percentile, based on age and sex)

    • Parent/primary caregiver willing to attend sessions with child

    Exclusion Criteria:
    • Failure to meet BMI criteria

    • Child with elevated internalizing or externalizing behavioral problems, as assessed through Child Behavior Checklist (CBCL)

    • Elevated parent distress, as measured by Symptom Checklist-90 (SCL-90)

    • Child on medications with any weight-altering effect

    • Inability to participate in moderate physical activity or attend study visits

    • Residing >1 hour from study site

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Pennsylvania Center for Weight and Eating Disorders Philadelphia Pennsylvania United States 19104

    Sponsors and Collaborators

    • University of Pennsylvania
    • Geisinger Center for Health Research
    • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

    Investigators

    • Principal Investigator: Myles S Faith, Ph.D., University of Pennsylvania

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Pennsylvania
    ClinicalTrials.gov Identifier:
    NCT01662557
    Other Study ID Numbers:
    • 807610
    • R34DK080473
    First Posted:
    Aug 10, 2012
    Last Update Posted:
    Aug 15, 2012
    Last Verified:
    Jan 1, 2011
    Keywords provided by University of Pennsylvania
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 15, 2012