- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01692314
Effect of Resistance Training on Microvascular, Hemodynamic and Physical Parameters in Obese Adolescents
September 24, 2012 updated by: Ingrid Barbara Ferreira Dias, Rio de Janeiro State University
Effect of Resistance Training on Microvascular Reactivity, Endothelial Function, Inflammatory Markers, Body Composition, Blood Pressure, Heart Rate and Physical Fitness in Obese Adolescents
The purpose of this study is to investigate the effect os resistance training on microvascular reactivity, endothelial functions, inflammatory markers, blood pressure, heart rate, body composition and physical fitness in obese adolescents.
Study Overview
Study Type
Interventional
Enrollment (Actual)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
RJ
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Rio de Janeiro, RJ, Brazil
- Laboratory for Clinical and Experimental Research in Vascular Biology (BioVasc), Biomedical Center, State University of Rio de Janeiro
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years to 17 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Tanner pubertal stage of development between three and five
- age between 13 up to 17 years old
Exclusion Criteria:
- presence of chronic diseases (diabetes mellitus, nephropathy and/or hypertension),
- musculoskeletal injury,
- smoking and
- to be in use of any medication.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Obese adolescents is being compared to control ones
Patients underwent to resistance training, three times a week, during three months.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Microvascular Reactivity
Time Frame: Three months
|
Three months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Endothelial function
Time Frame: Three months
|
Three months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Hemodynamic parameters
Time Frame: three months
|
three months
|
Imflammatory markers
Time Frame: three months
|
three months
|
Body composition
Time Frame: three months
|
three months
|
Physical fitness
Time Frame: three months
|
three months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Eliete Bouskela, Phd, State University of Rio de Janeiro
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2010
Primary Completion (Actual)
September 1, 2010
Study Completion (Actual)
May 1, 2012
Study Registration Dates
First Submitted
September 14, 2012
First Submitted That Met QC Criteria
September 24, 2012
First Posted (Estimate)
September 25, 2012
Study Record Updates
Last Update Posted (Estimate)
September 25, 2012
Last Update Submitted That Met QC Criteria
September 24, 2012
Last Verified
September 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BIOVASC 2009
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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