Trials / Suspended
SuspendedNCT04235842
Physical Exercise in Postoperative Bariatric Surgery Patients
Effects of Physical Exercise in Postoperative Bariatric Surgery Patients
- Status
- Suspended
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 75 (estimated)
- Sponsor
- Universidad Católica del Maule · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to determine the effect of two types of exercise training on body composition, cardiopulmonary function and quality of life in people after undergoing bariatric surgery.
Detailed description
Three groups will be studied: 1. Control group (CG) 2. Group of moderate intensity continuous aerobic exercise (GMICT) 3. High intensity interval aerobic exercise group (GHIIT) The CG will follow the usual protocol adopted by the hospital San Juan de Dios, Curicó, Chile. The protocol consists in delivering information about relevance of engage in regular physical exercise practice according to the World Health Organization (150 minutes of activity per week moderate physical or at least 75 minutes of intense physical activity), but do not include the patients in a supervised physical exercise program. The GMICT will undergo a physical exercise program in which the aerobic component will be a moderate-intensity continuous exercise training (60% of the heart rate reserve). The GHIIT will undergo the same exercise program of the GMICT, but the aerobic component will be a high-intensity interval exercise training (10 sets of 1 min at 90% of heart rate reserve, with 1 min of rest between sets). All groups will receive a nutritional diet plan prescribed by a specialist bariatric nutritionist blinded to the participants group assignment. At the end of the study, the CG will be invited to enjoy the exercise program showing to be more effective. Outcomes will be assessed at four time points: 1) one week before surgery; 2) 21 days after surgery (baseline before start exercise program); 3) 8 weeks after the beginning of the exercise program; and 4) one week after the end of intervention. Main outcomes are: 1) body composition; 2) heart rate variability; 3) six-minute walk test and 4) quality of life. Secondary outcomes will be: 1) maximal respiratory pressures; 2) flowmeter; 3) dynamometry of upper limb; and 4) squat test in 30 seconds. All procedures will be performed in the Hospital of Curicó, Chile, at the Department of Physical Medicine and Rehabilitation Service.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Physical Exercise | Moderate-intensity continuous exercise training performed at cycle ergometer. |
| OTHER | High-intensity interval training performed at cycle ergometer. | High-intensity interval training performed at cycle ergometer. |
Timeline
- Start date
- 2019-12-02
- Primary completion
- 2025-12-31
- Completion
- 2025-12-31
- First posted
- 2020-01-22
- Last updated
- 2024-04-16
Locations
1 site across 1 country: Chile
Source: ClinicalTrials.gov record NCT04235842. Inclusion in this directory is not an endorsement.