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Obesity Prevention for Pre-Adolescents
This study has been completed.
Sponsors and Collaborators: Stanford University
National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: Stanford University
ClinicalTrials.gov Identifier: NCT00185978
  Purpose

To develop and evaluate, in a randomized controlled trial, a comprehensive obesity prevention program for third, fourth and fifth grade students.

The intervention includes activities in THE SCHOOL, THE HOME, and a clinically oriented component for HIGH-RISK CHILDREN. In addition, the intervention will be delivered over a 3 year period, with age and grade-appropriate components for 3rd, 4th and 5th graders and their families. The primary outcome is body mass index.

PRIMARY OBJECTIVE: To significantly reduce body mass index, compared to controls, at the end of the three year intervention.


Condition Intervention Phase
Cardiovascular Diseases
Heart Diseases
Obesity
Behavioral: diet, physical activity, reduced sedentary behavior
Phase II

MedlinePlus related topics: Heart Diseases Obesity Obesity in Children
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Single Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: School- and Family-Based Obesity Prevention for Children

Further study details as provided by Stanford University:

Primary Outcome Measures:
  • body mass index

Secondary Outcome Measures:
  • prevalence/incidence of obesity
  • prevalence of obesity among high risk children
  • resting heart rate
  • moderate to vigorous physical activity
  • hours of television viewing
  • fat intake
  • preferences for low fat, high fiber foods
  • weight concerns
  • knowledge and attitudes

Estimated Enrollment: 900
Study Start Date: April 1998
Estimated Study Completion Date: March 2001
Detailed Description:

To develop and evaluate, in a randomized, controlled trial, a comprehensive obesity prevention program for third, fourth and fifth grade students.

Late childhood and early adolescence appears to be an important period in the development of obesity. Physiologic changes associated with puberty may increase the risk of acquiring clinically significant obesity. Onset of obesity in early adolescence appears to be associated with increased risks of "tracking" of obesity into adulthood, obesity-associated morbidity and mortality in adulthood, and obesity-associated psychosocial morbidity. However, (1) we have a limited ability to accurately identify those children who will become obese adults and those who will suffer obesity-related morbidities, (2) most existing treatments for overweight children and adolescents have yielded modest, unsustained effects, and (3) single-component preventive interventions have been relatively ineffective. Acknowledging these observations, the consensus at the recent NHLBI Strategy Development Workshop for Public Education on Weight and Obesity was that population-based primary and secondary prevention efforts, targeting pre-adolescents, may hold the greatest promise for addressing the problem of obesity. Therefore, we propose an integrated, multiple-component, school and family-based, primary and secondary prevention program targeting third, fourth and fifth graders.

Our proposed intervention model is derived directly from principles of Bandura's social cognitive theory. The intervention includes activities in THE SCHOOL, THE HOME, and a clinically oriented component for HIGH-RISK CHILDREN. In addition, the intervention will be delivered over a 3 year period, with age and grade-appropriate components for 3rd, 4th and 5th graders and their families.

We will evaluate the efficacy of our comprehensive intervention in a cohort of third graders, in ethnically diverse elementary schools. Schools will be randomly assigned to the comprehensive intervention or an attention-placebo curriculum, to minimize the potential for compensatory rivalry or resentful demoralization. Assessments of children's height, weight, triceps skinfold thickness, waist and hip circumferences, food preferences, cardio-respiratory fitness, and self-reported behavior, attitudes, and knowledge will occur every 6 months, and 6-months following the end of the intervention. The primary outcome is body mass index.

PRIMARY OBJECTIVE: To significantly reduce body mass index, compared to controls, at the end of the three year intervention.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • all third graders in the participating elementary schools at baseline

Exclusion Criteria:

  • unable to complete the study procedures
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00185978

Locations
United States, California
Stanford University School of Medicine
Stanford, California, United States, 94305
Sponsors and Collaborators
Stanford University
Investigators
Principal Investigator: Thomas N. Robinson, MD, MPH Stanford University
  More Information

Publications:
Robinson TN, Killen JD. Obesity prevention for children and adolescents. In: Thompson, J.K., & Smolak, L. (Eds.) Body Image, Eating Disorders, and Obesity in Youth: Assessment, Prevention, and Treatment. Washington, DC: American Psychological Association, 2001, pp. 261-292.

Study ID Numbers: R01 HL54102, R01 HL54102
Study First Received: September 12, 2005
Last Updated: September 12, 2005
ClinicalTrials.gov Identifier: NCT00185978  
Health Authority: United States: Federal Government

Keywords provided by Stanford University:
obesity prevention
preadolescents
schools

Study placed in the following topic categories:
Body Weight
Signs and Symptoms
Obesity
Heart Diseases
Nutrition Disorders
Overweight
Overnutrition

Additional relevant MeSH terms:
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 14, 2009