Home-based Exercise Training During Covid-19 Pandemic in Post-bariatric

  • STATUS
    Recruiting
  • participants needed
    70
  • sponsor
    University of Sao Paulo
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Updated on 5 August 2020
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covid-19
bariatric surgery

Summary

The aim of this study is to assess the effect of a home-based exercise training during social isolation due to covid-19 pandemic in patients who undertook bariatric surgery.

Description

Eligible patients will be invited to participate in the study by phone call. The research team will visit the included patients. All patients giving the written consent will perform the following tests before being randomly allocated into exercise training or control: 1) blood pressure; 2) anthropometric measures; 3) blood sampling; 4) handgrip test; 5) sit and stand test; 6) exercise capacity; 7) nutritional recalls and 8) health-related questionnaires. Patients will be randomized in a 1:1 ratio to control group (will receive information to keep active and eating healthy) or exercise training group (will receive a telemonitored exercise program through video conference, three times a week, during 4 months). Following 4 months of intervention, the outocomes will be re-assessed.

Details
Condition Gastric stapling, Obesity, Obesity
Age 18years - 80years
Treatment Home-based exercise
Clinical Study IdentifierNCT04425005
SponsorUniversity of Sao Paulo
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Men and women submitted to bariatric surgery in the last 12 months
Not engaged in regular exercise training programs

Exclusion Criteria

Patients with >12 months of post-operatory period
Patients with diagnosed mental disorders
Patients with physical limitations or not allowed by the physician to exercise
Patients infected with Covid-19 at the time of data collection
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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