The Impact of Resistance Exercise Training On Metabolic Dysregulation in Obese Children.
This study has been completed.
Sponsor:
McGill University Health Center
Information provided by:
McGill University Health Center
ClinicalTrials.gov Identifier:
NCT00460135
First received: April 11, 2007
Last updated: March 3, 2009
Last verified: March 2009
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Purpose
Impact of resistance training in prepubertal children with obesity focusing mostly in changes in body composition and markers of insulin resistance.
Hypothesis is that this will show positive changes in this randomized controlled trial.
| Condition | Intervention |
|---|---|
|
Childhood Obesity Body Composition Resistance Training Insulin Resistance |
Behavioral: resistance training |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | The Impact of Resistance Exercise Training On Metabolic Dysregulation in Obese Children. |
Resource links provided by NLM:
Further study details as provided by McGill University Health Center:
Primary Outcome Measures:
- Changes in body composition as per DEXA scans [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Changes in insulin resistance as per HOMA score [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
| Enrollment: | 20 |
| Study Start Date: | April 2006 |
| Study Completion Date: | July 2008 |
| Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: RT
resistance training
|
Behavioral: resistance training
2 times a week resistance training
|
|
No Intervention: Routine care
General counseling on increasing physical exercise
|
Detailed Description:
24 obese prepubertal obese children randomized to either resistance training program or usual care for 12 weeks. Baseline blood profiles and DEXA scans done before and after 12 weeks of training with the help of kinesiology graduates from Concordia University kinesiology department.
Eligibility| Ages Eligible for Study: | 8 Years to 12 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Between 8-12y
- Prepubertal
- Not on medications with known impact on weight loss
Exclusion Criteria:
- Pubertal
- Uncontrolled thyroid condition
- Type 2 diabetes
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00460135
Locations
| Canada, Quebec | |
| Montreal Children's Hospital | |
| Montreal, Quebec, Canada, H3H 1P3 | |
Sponsors and Collaborators
McGill University Health Center
Investigators
| Principal Investigator: | Laurent Legault, MD | Montreal Children's Hospital |
More Information
No publications provided
| Responsible Party: | Laurent Legault,MD, MUHC |
| ClinicalTrials.gov Identifier: | NCT00460135 History of Changes |
| Other Study ID Numbers: | PED-06-004 |
| Study First Received: | April 11, 2007 |
| Last Updated: | March 3, 2009 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by McGill University Health Center:
|
Resistance Training Obesity Children |
Additional relevant MeSH terms:
|
Insulin Resistance Obesity Hyperinsulinism Glucose Metabolism Disorders Metabolic Diseases |
Overnutrition Nutrition Disorders Overweight Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 19, 2013