Exercise Consultation in Obese Youth

NCT00722345 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2008-07-25

No results posted yet for this study

Summary

Exercise consultation, an intervention approach based on the transtheoretical model has been successful in promoting physical activity (PA) among adults. It is unknown whether this approach would be efficacious with youth. The purpose of this pilot study was to assess whether exercise consultation would increase PA levels and improve anthropometric measures and metabolic markers in obese adolescents.

Conditions

Interventions

BEHAVIORAL

review of "Canada's Physical Activity Guide for Youth"

The contents of the exercise booklet was reviewed with each participant of the control group by the research fellow. Health Canada's "Canada's Physical Activity Guide for Youth" was used for the exercise booklet

BEHAVIORAL

Exercise consultation

The exercise consultation consisted of a one-to-one discussion designed to educate the participant, strengthen his/her motivation and develop realistic goals and strategies to promote physical activity based on the patient's stage of change. The consultation was based upon the standardized protocol previously published by Loughlan and Mutrie. The Consultation Guidelines describe the 5 steps involved in an exercise consultation, including: 1) discussing current \& past activities; 2) reviewing the pros \& cons of exercising; 3) discussing the barriers to exercising and strategies for overcoming them; 4) determining the social support available to the patient; and finally, 5) setting realistic, attainable short term and long term goals to enhance physical activity.

Sponsors & Collaborators

  • St. Justine's Hospital

    lead OTHER

Principal Investigators

  • Melanie Henderson, MD MSc FRCP · Ste-Justine Hospital/McGill University

  • Celine Huot, MD MSc · Ste-Justine Hospital/University of Montreal

  • Denis Daneman, MB BCh FRCP · University of Toronto

  • Janet Hux, MD SM · University of Toronto

  • Anthony Hanley, PhD · University of Toronto

  • Jennifer McGrath, PhD MPH · Concordia University, Montreal

  • Marie Lambert, MD · Ste-Justine Hospital/University of Montreal

  • Gillian L Booth, MD MSc · University of Toronto

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-06-30
Primary Completion
2006-08-31
Completion
2006-08-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00722345 on ClinicalTrials.gov