Sedentary-time reduction and light activity plan to boost fitness before and after bariatric surgery
Official title: Targeting Sedentary Behavior Reduction and Physical Fitness Enhancement in Women Before and Beyond Bariatric Surgery- BARIMOV Study Protocol
Run by Hospital de Sao Sebastiao · NCT07663942 · Data updated 2026-11-12
This study tests whether a structured program to reduce sitting and increase light physical activity can improve fitness and post-surgery outcomes for women planning bariatric surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 72 (estimated) |
| Sponsor | Hospital de Sao Sebastiao Academic / other |
| Locations | 1 site (Santa Maria da Feira) |
| Status | Recruiting |
| Started | April 20, 2026 |
| Main results expected | October 20, 2030 |
| Study ends | April 20, 2031 |
| Registry record updated | June 23, 2026 |
| Trial ID | NCT07663942 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adult women (≥18 years) with BMI 30-45 kg/m2 scheduled for primary vertical sleeve gastrectomy or Roux-en-Y gastric bypass, who can consent and access digital tools.
✕Probably not a fit
Individuals unable to participate in physical activity testing or those with medical contraindications or diabetes may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
BARIMOV is a prospective cohort study in adult women with obesity planning bariatric surgery. Participants engage in an online sedentary behavior reduction program started about 6 months before surgery, with education and personalized guidance delivered via mobile apps. The study tracks five timepoints: baseline, just-before-surgery reassessment, during surgery for biopsies, and post-surgery follow-ups up to 12 months to examine physical fitness, surgical outcomes, and potential molecular changes in blood and tissues. It also explores how improvements in fitness might influence weight loss and related health factors after surgery. The approach combines behavioral intervention with biological sampling to understand mechanisms behind any observed effects.
Why it matters
Potential benefit: If successful, the program could help patients improve physical fitness and postoperative recovery after bariatric surgery.
How similar studies have gone: Prior research suggests lifestyle and activity interventions can influence surgical outcomes, but this specific pre/post-bariatric, biomarker-focused approach is exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult women (≥ 18 years); * BMI of 30-45 kg/m2; * Scheduled for primary vertical sleeve gastrectomy or Roux-en-Y gastric bypass; * Capacity to provide informed consent, adequate proficiency in the national language; * Access to the internet and mobile phone communication. Exclusion Criteria: * Previous bariatric surgery or gastric surgical procedure; * Physical incapacity or medical contraindications precluding physical fitness testing or participation (active cardiac disease, uncontrolled hypertension, severe joint disease); * Pregnancy or breastfeeding; * Inability to provide informed consent or comply with study procedures; * Patients with type 1 or 2 diabetes mellitus.
Where it's running
-
Unidade Local de Saúde de Entre Douro e Vouga
Santa Maria da Feira, Portugal Recruiting
Study contacts
- Study coordinator: Unidade Local de Saúde Entre Douro e Vouga
- Email: geral@ulsedv.min-saude.pt
- Phone: +351 256 379 700
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Weight-loss drugs tirzepatide vs. semaglutide in adults with obesity
This trial tests whether 12 weeks of tirzepatide or semaglutide have different effects on energy balance in adults with obesity but no diabetes.
-
Body composition changes after starting GLP-1 therapies in adults with obesity or type 2 diabetes
This study will follow adults with obesity and/or type 2 diabetes who are starting or adjusting a GLP-1 receptor agonist to see how their muscle and fat change over about a year.
-
Synbiotic for cognitive function in adults with obesity
A synbiotic containing Lactobacillus acidophilus and inulin is being tested to see if it improves cognitive function in adults with obesity and mild cognitive impairment.
-
Digital dietary help for people on GLP-1 therapy to reach better blood sugar and weight
This trial tests whether adding a digital dietary program (NutriSteppe) to usual care helps adults on GLP-1 medications see better blood sugar control and weight results.
-
Dramatherapy Added to Physical Activity for Obesity Care
This trial tests whether adding dramatherapy to a standard adapted physical activity program helps adults with obesity in bariatric or medical care improve psychosocial well‑being and weight-related outcomes.
-
Genetic predictors of weight loss with GLP-1/GIP therapies in obesity
This study tests whether a genetic risk score and specific obesity-related SNPs can predict how much weight adults with obesity will lose on semaglutide or tirzepatide.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.