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NCT07881770Not yet recruiting

Semaglutide Health Outcomes and Patient Adherence in Australia

Semaglutide Health Outcomes and Patient Adherence on Digital Health Platforms in Australia (SHAPED-AU)

Source: ClinicalTrials.gov · Last updated 19 Oct 2026

Brief summary (registry, in English)

This observational study aims to generate real-world evidence on the use of semaglutide in adults with overweight or obesity receiving care through a digital weight loss service (DWLS) programme in Australia. The study will evaluate treatment patterns, adherence, quality of life, safety, and other health outcomes associated with semaglutide use in routine clinical practice. Information will be collected from data generated during standard clinical care, and no study-specific treatment or procedures will be required.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
10000 (estimated)
First submitted
13 Oct 2026
Start date
13 Oct 2026
Primary completion date
28 Feb 2028
Lead sponsor
Novo Nordisk A/S
Diseases
Obesity
NCT number
NCT07881770

What you commit to

  • Study type: Observational
  • Planned participants: 10000
  • From 13 Oct 2026 to the primary completion date, 28 Feb 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous reported use of GLP-1 RA in the 3-month period before index date.
  • Are currently taking another obesity medication i.e. medication indicated for weight management treatment.
  • Any prior irreversible bariatric surgery for weight management

Other

  • Presence of a documented refusal to participate in research.

Who the study is looking for

  • Willing and able to provide informed consent
  • Greater than or equal to (\>=) 18 years of age at time of informed consent
  • Body Mass Index (BMI) \>= 27 kg/m2 and have \>= 1 excess weight-related comorbidity OR BMI \>= 30 kg/m2
  • Eligible to be prescribed semaglutide for the management of overweight or obesity
  • Have provided at least one weight measurement within 30 days of index date
  • Enrolled in existing Eucalyptus DWLS programme.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
SydneyAustraliaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.