A Multidisciplinary Weight Loss Program at AUB-MC

  • STATUS
    Recruiting
  • End date
    Dec 20, 2023
  • participants needed
    20
  • sponsor
    American University of Beirut Medical Center
Updated on 4 October 2022
metformin
behavior modification
dietary modification
obesity treatment
Accepts healthy volunteers

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.

Details
Condition Obesity, Weight Loss
Treatment Standard Care, Multidisciplinary weight loss program, Metformin Hcl 850Mg Tab
Clinical Study IdentifierNCT04194424
SponsorAmerican University of Beirut Medical Center
Last Modified on4 October 2022

Eligibility

Yes No Not Sure

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)
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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