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CompletedNCT07001553

Understanding Acute Dietary Changes After GLP-1 Agonist Treatment: The GLaD Feasibility Study

Understanding the Dietary Adjustments Following GLP-1 Agonist Treatment: The GLaD Feasibility Study

Status
Completed
Phase
Study type
Observational
Enrollment
37 (actual)
Sponsor
Australian Catholic University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

An observational study of those who have been prescribed a GLP-1 agonist therapy (yet to commence), for either weight or diabetes management, and are willing to complete dietary records and questionnaires of behaviour and psychosocial health.

Detailed description

Forty individuals (20 for weight management, 20 for diabetes management) living in Australia who have been prescribed a GLP-1 agonist (no previous prescription or no use in the previous 6 months) will be recruited to participate over the initial 3 months of their treatment. Assessments will occur remotely (online) at baseline, 2 weeks, 1 month and 3 months. Optional body composition assessments will be provided at baseline and 3 months for those based in Melbourne, Australia.

Conditions

Timeline

Start date
2025-05-28
Primary completion
2026-01-07
Completion
2026-01-07
First posted
2025-06-03
Last updated
2026-03-02

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT07001553. Inclusion in this directory is not an endorsement.

Understanding Acute Dietary Changes After GLP-1 Agonist Treatment: The GLaD Feasibility Study (NCT07001553) · Clinical Trials Directory