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

Status

Unknown

Conditions

Intervention / Treatment

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

Study Locations

  • Chile
    • 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
Other: HIIT
Group training with HIIT 3 times per week during 10 sessions
Experimental: Group Strength
Only Strength Training
Other: Strength
Group training with strength exercises 3 times per week during 10 sessions
Experimental: HIIT and Strength
Both intervention HIIT and Strength training
Other: HIIT
Group training with HIIT 3 times per week during 10 sessions
Other: Strength
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

University of Chile

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

Keywords

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.

Clinical Trials on Obesity

Clinical Trials on HIIT

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Montenegro

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe