MedPath

A Multidisciplinary Weight Loss Program at AUB-MC

Not Applicable
Active, not recruiting
Conditions
Obesity
Weight Loss
Interventions
Other: Standard Care
Other: Multidisciplinary weight loss program
Registration Number
NCT04194424
Lead Sponsor
American University of Beirut Medical Center
Brief Summary

The current project aims at evaluating the feasibility and efficacy of a multi-disciplinary weight loss program, using an innovative and simple dietary intervention at the American University of Beirut Medical Center (AUB-MC). Such intervention is expected to enhance patients' compliance and adherence to lifestyle changes. In addition, the program includes supervised exercise sessions and behavioral therapy. Therefore, our project proposes an evidence based approach to close the obesity treatment gaps.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Lebanese adult with obesity (≥18 years), obesity being defined as BMI ≥ 30 kg/m2
  • Patients who can commit to frequent visit trials as per study protocol
  • Patients not traveling outside Lebanon for at least the 6-month period of the trial
  • Patients tolerating Metformin after a run-in period of 2 weeks
Exclusion Criteria
  • Patients who have taken other weight reducing drug therapy in the previous 6 months
  • Patients who have undergone bariatric therapy or endoscopic procedure, or planning to do so in the near future (at < 6 months)
  • Patients with diabetes
  • Patients working at AUB-MC, as we will not be able to assess the adherence to study visits nor the feasibility of such a program in the general population, presenting to AUB-MC only for clinical care
  • A family member of a patient already enrolled in the study, as the participants will not be independent
  • Pregnant obese patients
  • Patients with pacemakers
  • Patients known to have hypertension, cardiac, pulmonary, renal or liver disease, active cancer or psychiatric illnesses
  • History of any surgery of less than 6 weeks duration
  • Patients known to have disabling osteoarthritic or orthopedic problems
  • Patients secondary uncontrolled endocrine disorders (thyroid disorders, polycystic ovary, Cushing disease), or drug induced obesity (such as anti-psychotic, steroids, hormonal therapy).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Multidisciplinary programMetformin Hcl 850Mg TabMultidisciplinary weight loss program
ControlStandard CareStandard care
Multidisciplinary programMultidisciplinary weight loss programMultidisciplinary weight loss program
ControlMetformin Hcl 850Mg TabStandard care
Primary Outcome Measures
NameTimeMethod
Mean percent weight loss per treatment arm6 months after enrollment

\[(baseline weight-follow up weight at 6 months)/ baseline weight\] X 100

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

American University of Beirut - Medical Center

🇱🇧

Beirut, Riad El Solh, Lebanon

© Copyright 2025. All Rights Reserved by MedPath