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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00739180
Other study ID # 7-08-JF-27
Secondary ID
Status Completed
Phase N/A
First received August 20, 2008
Last updated November 2, 2012
Start date November 2007
Est. completion date October 2011

Study information

Verified date October 2012
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

In this randomized controlled trial, we will examine the effect of a 3-month exercise training (aerobic exercise versus resistance exercise) without calorie restriction on total and regional adiposity, and risk of type 2 diabetes in overweight children and adolescents.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria:

- Healthy overweight (BMI >-95th) youth between 12 and 18 years of age

- Waist circumference >-75th percentile

- Sedentary (no structured exercise >2 times/week for past 6 months)

- Non-smokers, non-diabetic, no medical conditions

- Weight stable for past 3 months

Exclusion Criteria:

- Smokers,

- diabetic,

- psychiatric disorders,

- syndromatic obesity

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Control
Standard care control (no exercise)
Resistance Exercise
Supervised resistance exercise using stack weight equipments.
Aerobic exercise
Supervised aerobic exercise using treadmills, bikes, and ellipticals

Locations

Country Name City State
United States Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine Pittsburgh Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
University of Pittsburgh American Diabetes Association

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Abdominal obesity, visceral fat 3 month No
Secondary Insulin sensitivity and secretion, glucose tolerance 3 month No
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