Physical Activity and Bariatric Surgery (ACTIBARIA)

September 17, 2021 updated by: Centre Hospitalier Régional d'Orléans

Effects of Controlled Physical Activity on the Fitness, Body Composition and Quality of Life of Obese Women Undergoing Bariatric Surgery

Bariatric surgery indeed leads to significant weight loss, reduces mortality risk, obesity-associated comorbidities (Wolfe et al., 2016) and improves functional physical abilities (Herring et al., 2016). Because these benefits are related to decreased energy intake, the investigators aim to optimize them by combining them with supervised adapted physical activity practice.

So, the aim of this clinical trial is to measure the effects of a physical training program on physical fitness, body composition and quality of life of obese women who have undergone bariatric surgery.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Upon hospitalization for their bariatric surgery (bypass or sleeve), subjects will sign their informed consent and be included in the study. Six weeks' post-surgery, the subjects will be randomized in one of the 2 groups (Control group CG or Adapted Physical Activity group APAG). Patients in both groups will have 3 postoperative visits one at 6 weeks (V1), one at 18 weeks (V2) and one at 30 weeks (V3). During these visits, they will undergo the same assessments (body composition, physical condition, quality of life). Patients in the CG will receive standard hospital management. Patients in APAG will follow the same management and will also follow a 3-month physical activity program 3 times a week between V1 and V2. Then, between V2 and V3, no APA program will be offered to both groups.

The subjects will evaluate during each visit V1, V2 and V3:

  • body composition,
  • physical condition,
  • quality of life
  • daily physical activity

Study Type

Interventional

Enrollment (Actual)

37

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 Locations

      • Orleans 2, France, 45067
        • CHR Orléans

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 55 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • women between 18 and 55 years old
  • undergoing bariatric surgery (a "bypass gastric" or a "sleeve")
  • not practicing a supervised physical activity
  • having read and signed an informed consent prior to the start of the trial
  • being affiliated to a social security system

Exclusion Criteria:

  • Women with a contraindication to physical activity
  • any medical contraindication to the practice of stress tests.
  • unable to go to the hospital regularly
  • having a significant functional limitation that does not allow her to perform the 6-minute walk test
  • with an intellectual disability and/or psychiatric illness
  • does not speak and/or understand French
  • pregnant woman
  • under guardianship or curatorship
  • participating in another clinical research

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Adapted Physical Activity Group
Patients will follow a 3-month physical activity program 3 times a week between V1 and V2. Then, between V2 and V3, no APA program will be offered to both groups.
Between V1 and V2 (i.e. 12 weeks), the APAG (Adapted Physical Activity Group) will participate at a physical training program, 3 sessions of 1h30 per week consisting of endurance activities (60-75% of VO2 peak) and muscle strengthening while the CG will not perform any controlled physical training program. Then, between V2 and V3, no APA (Adapted Physical Activity) program will be offered to both groups.
No Intervention: Control group
Patients will receive standard hospital management

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximum oxygen consumption (VO2 max)
Time Frame: Week 6
The VO2 max is measured during an effort test with progressively increasing and maximum load which consists in making the subject pedal against an increasing load
Week 6
Maximum oxygen consumption (VO2 max)
Time Frame: Week 18
The VO2 max is measured during an effort test with progressively increasing and maximum load which consists in making the subject pedal against an increasing load
Week 18
Maximum oxygen consumption (VO2 max)
Time Frame: Week 30
The VO2 max is measured during an effort test with progressively increasing and maximum load which consists in making the subject pedal against an increasing load
Week 30

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of obesity on the physical, psycho-social, dietary well-being and dieting experience assessed using the Quality of Life, Obesity and Diet Scale (QOLDS)
Time Frame: Week 6
QoL will be assessed using a simplified version of the French obesity-specific QoL questionnaire developed by Ziegler et al. Each participant will be asked to evaluate 14 statements about their life on a 4-point Likert scale (with 1 representing total disagreement and 4 representing total agreement). The 14 statements (eg, "Because of my weight, I have trouble to dress or undress") will equally be divided between physical aspects of life and psychosocial aspects of life. A French obesity-specific QoL questionnaire will be used to calculate the participants' physical dimension of QoL scores and psychoso-cial dimension of QoL scores by summing the points for each relevant item (range: 7-28 points). The total score will also be calculated (range: 14-56 points). The higher the scores, the better the QoL.
Week 6
Impact of obesity on the physical, psycho-social, dietary well-being and dieting experience assessed using the Quality of Life, Obesity and Diet Scale (QOLDS)
Time Frame: Week 18
QoL will be assessed using a simplified version of the French obesity-specific QoL questionnaire developed by Ziegler et al. Each participant will be asked to evaluate 14 statements about their life on a 4-point Likert scale (with 1 representing total disagreement and 4 representing total agreement). The 14 statements (eg, "Because of my weight, I have trouble to dress or undress") will equally be divided between physical aspects of life and psychosocial aspects of life. A French obesity-specific QoL questionnaire will be used to calculate the participants' physical dimension of QoL scores and psychoso-cial dimension of QoL scores by summing the points for each relevant item (range: 7-28 points). The total score will also be calculated (range: 14-56 points). The higher the scores, the better the QoL.
Week 18
Impact of obesity on the physical, psycho-social, dietary well-being and dieting experience assessed using the Quality of Life, Obesity and Diet Scale (QOLDS)
Time Frame: Week 30
QoL will be assessed using a simplified version of the French obesity-specific QoL questionnaire developed by Ziegler et al. Each participant will be asked to evaluate 14 statements about their life on a 4-point Likert scale (with 1 representing total disagreement and 4 representing total agreement). The 14 statements (eg, "Because of my weight, I have trouble to dress or undress") will equally be divided between physical aspects of life and psychosocial aspects of life. A French obesity-specific QoL questionnaire will be used to calculate the participants' physical dimension of QoL scores and psychoso-cial dimension of QoL scores by summing the points for each relevant item (range: 7-28 points). The total score will also be calculated (range: 14-56 points). The higher the scores, the better the QoL.
Week 30
Walking distance
Time Frame: Week 6
The walking distance (meters) will be evaluated during the 6 minutes walk test
Week 6
Walking distance
Time Frame: Week 18
The walking distance (meters) will be evaluated during the 6 minutes walk test
Week 18
Walking distance
Time Frame: Week 30
The walking distance (meters) will be evaluated during the 6 minutes walk test
Week 30
Heart rate
Time Frame: Week 6
The heart rate (beats/min) will be evaluated during the 6 minutes walk test
Week 6
Heart rate
Time Frame: Week 18
The heart rate (beats/min) will be evaluated during the 6 minutes walk test
Week 18
Heart rate
Time Frame: Week 30
The heart rate (beats/min) will be evaluated during the 6 minutes walk test
Week 30
Perception of the effort
Time Frame: Week 6
This will be evaluated with a Borg scale (the minimum score is 0 = no exertion and the maximal 10 = maximal exertion) at the end of the 6-minutes walk test.
Week 6
Perception of the effort
Time Frame: Week 18
This will be evaluated with a Borg scale (the minimum score is 0 = no exertion and the maximal 10 = maximal exertion) at the end of the 6-minutes walk test.
Week 18
Perception of the effort
Time Frame: Week 36
This will be evaluated with a Borg scale (the minimum score is 0 = no exertion and the maximal 10 = maximal exertion) at the end of the 6-minutes walk test.
Week 36
Maximum voluntary force of the quadriceps
Time Frame: week 6

The maximum voluntary isometric strength of the knee extensors (strength of quadriceps in kilograms) will be measured with a MicroFET2 handheld dynamometer.

Each participant's lower extremity could be placed in a position a knee flexion of 90 degrees. They will be asked to apply maximal force against the dynamometer held by the physical therapist. Before the test, the participants will be given a standard instruction of "push as hard as you can." Encouragement to apply maximal effort will also be given during the test. Each participant will be instructed to exert maximal strength for 3-5 seconds until the examiner instructed the patient to relax.

week 6
Maximum voluntary force of the quadriceps
Time Frame: week 18

The maximum voluntary isometric strength of the knee extensors (strength of quadriceps in kilograms) will be measured with a MicroFET2 handheld dynamometer.

Each participant's lower extremity could be placed in a position a knee flexion of 90 degrees. They will be asked to apply maximal force against the dynamometer held by the physical therapist. Before the test, the participants will be given a standard instruction of "push as hard as you can." Encouragement to apply maximal effort will also be given during the test. Each participant will be instructed to exert maximal strength for 3-5 seconds until the examiner instructed the patient to relax.

week 18
Maximum voluntary force of the quadriceps
Time Frame: week 30

The maximum voluntary isometric strength of the knee extensors (strength of quadriceps in kilograms) will be measured with a MicroFET2 handheld dynamometer.

Each participant's lower extremity could be placed in a position a knee flexion of 90 degrees. They will be asked to apply maximal force against the dynamometer held by the physical therapist. Before the test, the participants will be given a standard instruction of "push as hard as you can." Encouragement to apply maximal effort will also be given during the test. Each participant will be instructed to exert maximal strength for 3-5 seconds until the examiner instructed the patient to relax.

week 30
grip strength
Time Frame: week 6
The grip strength will be evaluated with a dynamometer that can be squeezed very hard for 3 seconds. The measurement will be evaluated three times with 30 seconds of recovery and the maximum value will be retained.
week 6
grip strength
Time Frame: week 18
The grip strength will be evaluated with a dynamometer that can be squeezed very hard for 3 seconds. The measurement will be evaluated three times with 30 seconds of recovery and the maximum value will be retained.
week 18
grip strength
Time Frame: week 30
The grip strength will be evaluated with a dynamometer that can be squeezed very hard for 3 seconds. The measurement will be evaluated three times with 30 seconds of recovery and the maximum value will be retained.
week 30
Body composition
Time Frame: week 6
Body composition will be assessed by a body composition analyser in the morning on an empty stomach
week 6
Body composition
Time Frame: week 18
Body composition will be assessed by a body composition analyser in the morning on an empty stomach
week 18
Body composition
Time Frame: week 30
Body composition will be assessed by a body composition analyser in the morning on an empty stomach
week 30
Metabolic measurements
Time Frame: week 6

During the constant workload exercise, blood samples will be taken and metabolic measurements will be made:

- Blood Lactate (mmol/L)

week 6
Metabolic measurements
Time Frame: week 6

During the constant workload exercise, blood samples will be taken and metabolic measurements will be made:

- Blood glucose (g/L)

week 6
Hormonal measurements
Time Frame: week 6

During the constant workload exercise, blood samples will be taken and hormonal measurements will be made:

  • Testosterone (ng/ml)
  • Cortisol (ng/ml)
week 6
Metabolic measurements
Time Frame: week 18

During the constant workload exercise, blood samples will be taken and metabolic measurements will be made:

- Blood glucose (g/L)

week 18
Metabolic measurements
Time Frame: week 18

During the constant workload exercise, blood samples will be taken and metabolic measurements will be made:

- Blood Lactate (mmol/L)

week 18
Hormonal measurements
Time Frame: week 18

During the constant workload exercise, blood samples will be taken and hormonal measurements will be made:

  • Testosterone (ng/ml)
  • Cortisol (ng/ml)
week 18
Metabolic measurements
Time Frame: week 30

During the constant workload exercise, blood samples will be taken and metabolic measurements will be made:

- Blood glucose (g/L)

week 30
Metabolic measurements
Time Frame: week 30

During the constant workload exercise, blood samples will be taken and metabolic measurements will be made:

- Blood Lactate (mmol/L)

week 30
Hormonal measurements
Time Frame: week 30

During the constant workload exercise, blood samples will be taken and hormonal measurements will be made:

  • Testosterone (ng/ml)
  • Cortisol (ng/ml)
week 30

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Virgile AMIOT, Dr, CHR d'Orléans

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Actual)

February 23, 2018

Primary Completion (Actual)

June 7, 2021

Study Completion (Actual)

June 7, 2021

Study Registration Dates

First Submitted

July 22, 2021

First Submitted That Met QC Criteria

September 17, 2021

First Posted (Actual)

September 21, 2021

Study Record Updates

Last Update Posted (Actual)

September 21, 2021

Last Update Submitted That Met QC Criteria

September 17, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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