Physical Condition and Bariatric Surgery (CaPaCITy)

  • STATUS
    Recruiting
  • End date
    Oct 22, 2023
  • participants needed
    150
  • sponsor
    University Hospital, Clermont-Ferrand
Updated on 3 March 2022

Summary

The aim of this project is to investigate in obese patients the changes induced by bariatric surgery on the various components of the physical condition and their postoperative evolution following an intervention combining a physical activity program (aquabike vs bicycle) with or without protein supplementation.

Description

Physical condition will be evaluated in obese patients before surgery and 1, 4, 6, 12, 18 and 24 months after surgery.

Between 1 and 4 months after surgery, participants will be assigned to one of the postoperative care groups:

  • Control
  • Control + protein supplementation
  • Training in aquabike
  • Training in aquabike + protein supplementation
  • Bicycle training
  • Bicycle training + protein supplementation

Details
Condition Obese Patients With Bariatric Surgery
Treatment Physical activity program : aquabike, Physical activity program : bicycle, Physical activity program : with protein supplementation, Physical activity program : without protein supplementation
Clinical Study IdentifierNCT03197857
SponsorUniversity Hospital, Clermont-Ferrand
Last Modified on3 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Male or Female
Age between 18 and 60 years
Body mass index: BMI> 40 kg / m2
Candidates for bariatric surgery

Exclusion Criteria

Subject under 18 or over 60 years of age
Biological assessment considered abnormal by the investigator
HIV serology or known positive HCV
Pregnant or nursing women
For women of childbearing age: beta-hCG positive dosage or absence of contraception deemed reliable (oral contraceptive, IUD, implant or hormonal patch)
Medical or surgical history (judged by the investigator to be inconsistent with the study)
Subject with cardiorespiratory and / or osteo-articular disorders limiting their ability to perform physical tests or training
Subject with cardiovascular or neoplastic disease
Subjects with an infection in the 3 months prior to inclusion
Hypercorticism and uncontrolled dysthyroidism
Patient with known neuro-muscular pathology: myopathy, myasthenia gravis, rhabdomyolysis, paraplegia, hemiplegia
Patient with chronic or acute inflammatory disease the 3 months before inclusion
CRP> 20 mg / l
Person treated with or having stopped treatment for less than 3 months prior to inclusion by corticosteroids, immunosuppressant, anabolic agent, growth hormone
Person with an unstable psychiatric condition
Blood donation in the two months preceding the study
High alcohol consumption (> 2 to 3 drinks per day depending on sex) or presence of drug addiction
Significant smoking (> 5 cigarettes / day or equivalent in cigars or pipe tobacco)
Intense sports activity (> 5 hours / week)
Subjects excluded from another study or having received more than 4500 in the year following their participation in clinical studies
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

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.

Learn more

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

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note