Effects of High Intensity Interval Training and Strength Training in Obese

Obesity Clinical Trial

— EHITSTR  

Official title:

Effects of High Intensity Interval Training, Strength Training and the Combination in Overweight and Obese

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02484235
• Other study ID #: pro-001
• Status: Recruiting
• Phase: N/A
• First received: June 23, 2015
• Last updated: June 25, 2015
• Start date: June 2015
• Est. completion date: March 2016

Study information

• Verified date: June 2015
• Source: University of Chile
• Contact: Marcelo Cano, PhD
• Phone: 29786513
• Email: mcano[@]med.uchile.cl
• Is FDA regulated: No
• Health authority: Chile: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: March 2016
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Obesity

Intervention

Other:
• HIIT
Group training with HIIT 3 times per week during 10 sessions
• Strength
Group training with strength exercises 3 times per week during 10 sessions

Locations

Country	Name	City	State
Chile	Hospital Clinico de la Universidad de Chile	Santiago	Metropolitana

Sponsors (1)

Lead Sponsor	Collaborator
University of Chile

Country where clinical trial is conducted

Chile, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Exercise Test of Vo2 kinetics		6 weeks	No
Secondary	Strength test of 10 maximum repetition (10RM)		6 weeks	No
Secondary	Exercise test of max Walking Speed		6 weeks	No