Targeted Obesity Prevention Program for Adolescent Females

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Oregon Research Institute
ClinicalTrials.gov Identifier:
NCT00433680
First received: February 9, 2007
Last updated: April 7, 2014
Last verified: April 2014
  Purpose

The purpose of this study is to evaluate the effectiveness of an obesity prevention program when administered to female college freshmen.


Condition Intervention
Obesity
Behavioral: Healthy Weight

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Investigator)
Primary Purpose: Prevention
Official Title: Targeted Obesity Prevention Program for Adolescent Females

Resource links provided by NLM:


Further study details as provided by Oregon Research Institute:

Primary Outcome Measures:
  • risk for future onset of obesity and weight gain [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • measure changes in caloric intake, physical activity, and body dissatisfaction [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 405
Study Start Date: March 2007
Study Completion Date: March 2012
Primary Completion Date: March 2012 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: Healthy Weight
    4 weekly 1 hour meetings that encourage reductions in fat and sugar intake and increases in physical activity to decrease onset of obesity and body dissatisfaction.
    Other Name: Healthy Weight Project
  Show Detailed Description

  Eligibility

Ages Eligible for Study:   17 Years to 19 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All female college freshmen at the University of Oregon will be invited to participate in the study.

Exclusion Criteria:

  • Any participant that meets criteria for an eating disorder at any assessment point will be excluded from the study.
  • Any participant with BMI below 5% for their age group will be excluded to avoid health risks
  • Any participant who does not report some form of body dissatisfaction will be excluded from the study
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00433680

Locations
United States, Oregon
Oregon Research Institute
Eugene, Oregon, United States, 97403
Sponsors and Collaborators
Oregon Research Institute
Investigators
Principal Investigator: Eric Stice, PhD Oregon Research Institute
  More Information

Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Oregon Research Institute
ClinicalTrials.gov Identifier: NCT00433680     History of Changes
Other Study ID Numbers: DK72932, R01DK072932
Study First Received: February 9, 2007
Last Updated: April 7, 2014
Health Authority: United States: Federal Government

Keywords provided by Oregon Research Institute:
adolescent
female
obesity
body dissatisfaction

Additional relevant MeSH terms:
Obesity
Body Weight
Nutrition Disorders
Overnutrition
Overweight
Signs and Symptoms

ClinicalTrials.gov processed this record on October 20, 2014