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Official title Concurrent Exercise Effects in Post-Bariatric Patients
ClinicalTrials.gov ID: NCT07423780
What this study is testing
- What it's testing
- This study aims to evaluate the effect of a 5-week concurrent exercise program (aerobic and resistance training) on muscle quality, body composition, functional response, and quality of life in individuals undergoing bariatric surgery. This is a single-center, prospective, longitudinal, non-randomized controlled clinical trial with two groups: intervention and control.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 60
You may be able to join if
- Voluntarily agree to participate and sign informed consent.
- Men and women aged 18 to 60 years.
- Have undergone bariatric surgery (sleeve gastrectomy or gastric bypass) at BUPA Clinic Santiago.
- Have a medical indication for metabolic rehabilitation.
- May present associated comorbidities such as insulin resistance syndrome, dyslipidemia, arterial hypertension, and/or hypothyroidism.
You likely can't join if
- Diagnosis of type 1 or type 2 diabetes mellitus.
- Severe musculoskeletal disorders that impair ambulation or limit participation in the exercise program.
- History of a cardiovascular event.
- Severe cardiorespiratory diseases that significantly reduce physical capacity or cause dyspnea at rest or with minimal exertion.
- Dependence on supplemental oxygen.
- Bariatric surgery-related complications, including:
See the full eligibility criteria
- Voluntarily agree to participate and sign informed consent.
- Men and women aged 18 to 60 years.
- Have undergone bariatric surgery (sleeve gastrectomy or gastric bypass) at BUPA Clinic Santiago.
- Have a medical indication for metabolic rehabilitation.
- May present associated comorbidities such as insulin resistance syndrome, dyslipidemia, arterial hypertension, and/or hypothyroidism.
- Diagnosis of type 1 or type 2 diabetes mellitus.
- Severe musculoskeletal disorders that impair ambulation or limit participation in the exercise program.
- History of a cardiovascular event.
- Severe cardiorespiratory diseases that significantly reduce physical capacity or cause dyspnea at rest or with minimal exertion.
- Dependence on supplemental oxygen.
- Bariatric surgery-related complications, including:
- Staple line leak or fistula
- Hemorrhage/bleeding
- Stenosis or gastric narrowing/stricture
- Intra-abdominal abscess
- Hypersensitivity (as clinically determined).
- Hepatic and/or renal insufficiency.
The study team makes the final eligibility decision.
Where it's taking place
- Santiago, Santiago Metropolitan, Chile
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 60 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Santiago, Santiago Metropolitan, Chile. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.