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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02143453
Other study ID # HIIT in Juvenile Obesity
Secondary ID
Status Completed
Phase N/A
First received May 18, 2014
Last updated May 20, 2014
Start date August 2010
Est. completion date August 2011

Study information

Verified date May 2014
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

Exercise is an effective strategy to manage juvenile obesity; however this ideal exercise training mode is still unclear. In this study, the investigators compared the health-related effects of high intensity interval training versus endurance training in obese children.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender Both
Age group 8 Years to 12 Years
Eligibility Inclusion Criteria:

- age between 8 and 12 years

- Body mass index (BMI) = 95th percentile, according to the First National Health and Nutrition Examination Survey

- no pharmacological treatment

- no evidence of metabolic, hormonal, orthopedic, and cardiovascular disease at the time of the study's commencement

- no participation in any regular exercise training program (except physical education classes, two days a week) at least 6 months before the commencement of the study and throughout the protocol.

Exclusion Criteria:

- non-obese participants

- physically active participants

- participants with cardiovascular diseases or any other condition that could preclude the participation in the the exercise training program

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
Endurance training
30 to 60-minute continuous exercise at 80% of the peak heart rate
High intensity interval training
3 to 6 sets of 60-second sprints at 100% of the peak velocity interspersed by a 3-min active recovery period.

Locations

Country Name City State
Brazil General Hospital (School of Medicine, University of Sao Paulo) Sao Paulo

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary body mass index (BMI) 12 weeks No
Primary aerobic conditioning (VO2max) 12 weeks No
Primary insulin sensitivity (HOMA-index) 12 weeks No
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