Kid STRIDE: Exploring Participation in a Family-based Intervention

This study has been completed.
Sponsor:
Information provided by:
University of Wisconsin, Madison
ClinicalTrials.gov Identifier:
NCT00682422
First received: May 16, 2008
Last updated: June 30, 2010
Last verified: June 2010
  Purpose

The aim of this qualitative study is to explore parental and child perceptions of participating in a family-based behavioral intervention targeting healthy behaviors.


Condition
Obesity

Study Type: Observational
Study Design: Observational Model: Family-Based
Time Perspective: Retrospective
Official Title: Kid STRIDE: Exploring Participation in a Family-based Intervention

Resource links provided by NLM:


Further study details as provided by University of Wisconsin, Madison:

Primary Outcome Measures:
  • Explore parental and child perceptions of participating in a family-based behavioral intervention targeting weight reduction. [ Time Frame: After completion of primary group intervention. ] [ Designated as safety issue: No ]

Enrollment: 10
Study Start Date: February 2008
Study Completion Date: June 2008
Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts
Parent & Child Dyad

Detailed Description:

Children ages 9-14 have been participating in the Kid STRIDE study which is a family-based behavioral intervention for obese children. Participants will be divided into 3 groups according to their change in weight: 1) children who lost greater than 5% of body weight; 2) children who lost less than 5% of body weight or gained less than 1% of body weight; 3) children who gained greater than 1% of body weight. We will invite five families from each of groups 1 and 3 to participate in an open-ended interview.

  Eligibility

Ages Eligible for Study:   9 Years to 16 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Participants in the current Kid STRIDE behavioral intervention study.

Criteria

Inclusion Criteria:

  • Completed the 15-week primary intervention phase of Kid STRIDE
  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: NCT00682422

Locations
United States, Wisconsin
University of Wisconsin
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
University of Wisconsin, Madison
Investigators
Principal Investigator: Ellen R Wald, MD University of Wisconsin, Madison
  More Information

Publications:
Responsible Party: Ellen R. Wald, MD, University of Wisconsin
ClinicalTrials.gov Identifier: NCT00682422     History of Changes
Other Study ID Numbers: M-2007-1471
Study First Received: May 16, 2008
Last Updated: June 30, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by University of Wisconsin, Madison:
pediatrics, overweight, obese, behavioral intervention

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

ClinicalTrials.gov processed this record on August 21, 2014