Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

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.

More Obesity (Disorder) trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment72 (estimated)
SponsorHospital de Sao Sebastiao
Academic / other
Locations1 site (Santa Maria da Feira)
StatusRecruiting
StartedApril 20, 2026
Main results expectedOctober 20, 2030
Study endsApril 20, 2031
Registry record updatedJune 23, 2026
Trial IDNCT07663942 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

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.