- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02484235
Effects of High Intensity Interval Training and Strength Training in Obese (EHITSTR)
June 25, 2015 updated by: Edgardo Opazo, University of Chile
Effects of High Intensity Interval Training, Strength Training and the Combination in Overweight and Obese
Obesity is a global health problem since it is associated with many cardiovascular and metabolic diseases, osteoarticular problems and some cancers.
That is why it is a priority of the national health policies.
Exercise is a mainstay in the treatment, but still the most effective method is sought.
The resistance exercise and high intensity intervals (HIIT) have been shown to positively affect the outcome of the disease, increasing the oxidative capacity of the trained subjects.
Therefore it is important to look if both together produce greater benefits or otherwise nullify its effects, such as suggested by recent publications in relation to the cellular response to different stimuli such exercise in skeletal muscle.
The aim of this study is to evaluate the effectiveness of interventions exercise high intensity intervals, overload and combining them in the oxidative capacity of obese subjects.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
30
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 Contact
- Name: Marcelo Cano, PhD
- Phone Number: 29786513
- Email: mcano@med.uchile.cl
Study Locations
-
-
Metropolitana
-
Santiago, Metropolitana, Chile
- Recruiting
- Hospital Clinico de la Universidad de Chile
-
Contact:
- Ariel Castro
- Phone Number: +56 2 2978 8535
- Email: oaic@hcuch.cl
-
-
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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Indication of medical supervised exercise
- BMI of 25-35kg/m2
- Participate in a 10 session rehabilitation program
Exclusion Criteria:
- Osteomuscular injuries
- Cardiovascular disease without control
- Bariatric Surgery
- High blood pressure without control
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group HIIT
Only Aerobic Training with HIIT
|
Group training with HIIT 3 times per week during 10 sessions
|
Experimental: Group Strength
Only Strength Training
|
Group training with strength exercises 3 times per week during 10 sessions
|
Experimental: HIIT and Strength
Both intervention HIIT and Strength training
|
Group training with HIIT 3 times per week during 10 sessions
Group training with strength exercises 3 times per week during 10 sessions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Exercise Test of Vo2 kinetics
Time Frame: 6 weeks
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Strength test of 10 maximum repetition (10RM)
Time Frame: 6 weeks
|
6 weeks
|
Exercise test of max Walking Speed
Time Frame: 6 weeks
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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, 2015
Primary Completion (Anticipated)
December 1, 2015
Study Completion (Anticipated)
March 1, 2016
Study Registration Dates
First Submitted
June 23, 2015
First Submitted That Met QC Criteria
June 25, 2015
First Posted (Estimate)
June 29, 2015
Study Record Updates
Last Update Posted (Estimate)
June 29, 2015
Last Update Submitted That Met QC Criteria
June 25, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PRO-001
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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