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Taking people in AlgeriaNo phase

Multidisciplinary Obesity Care Programme With Semaglutide and Behavioral Treatment in Adults

Tests a team-based obesity care programme, including semaglutide, in adults living with obesity.

Plain-language title generated from the registry record
Registry title: OBESIAL: A Prospective Interventional Real-world Study of a Multidisciplinary Obesity Management Programme

Key facts

Where
Algiers, AlgeriaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07779343, who can take part

Where in Algeria

  • Department of Medicine, , Mother and Child Hospital of the Army (MCHA), Algiers University Hospital, Algiers, Algeria.Algiers, AlgeriaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Health Sciences, Algeria
Trial code
NCT07779343
Record updated
21 August 2026
Original description
The OBESIAL (Obesity Structured Intervention in Algeria) study aims to evaluate the clinical, metabolic, and organisational impact of a structured multidisciplinary obesity care pathway implemented under real-world conditions.Read full original descriptionShow less

OBESIAL: A Prospective Interventional Real-world Study of a Multidisciplinary Obesity Management Programme

The OBESIAL (Obesity Structured Intervention in Algeria) study aims to evaluate the clinical, metabolic, and organisational impact of a structured multidisciplinary obesity care pathway implemented under real-world conditions.

Inclusion: Adults aged 18-65 years; BMI ≥30 kg/m²; Written informed consent obtained prior to enrolment.

Exclusion: Previous bariatric surgery; Obesity pharmacotherapy within the previous 90 days; Severe or unstable comorbidities compromising safety or participation, including:; Recent acute cardiovascular event (<60 days); Active malignancy; Severe unstable organic disease; Severe unstable psychiatric disorders; Genetic obesity or obesity secondary to uncontrolled endocrine disease; Refusal to participate or inability to adhere to follow-up procedures; Pregnancy at enrolment; Known contraindication to planned therapeutic options; Pregnancy occurring during follow-up; Initiation of chronic treatment associated with weight gain.

ClinicalTrials.gov NCT07779343