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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01323088
Other study ID # 1R21DK083654-01A1
Secondary ID
Status Completed
Phase N/A
First received March 22, 2011
Last updated April 12, 2013
Start date August 2010
Est. completion date October 2012

Study information

Verified date April 2013
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, ectopic fat in the liver and skeletal muscle, and risk of type 2 diabetes in overweight girls.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date October 2012
Est. primary completion date October 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
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

- Diabetes

- Psychiatric disorders

- Syndromic obesity

- Pregnancy

- Taking medications known to affect study outcomes

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 (1)

Lead Sponsor Collaborator
University of Pittsburgh

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 by a 3-hour hyperinsulinemic-euglycemic clamp, oral glucose tolerance test, liver fat and intramyocellular lipid by 1H-magnetic resonance spectroscopy. 3 month No
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