Understanding Acute Dietary Changes After GLP-1 Agonist Treatment: The GLaD Feasibility Study
Launched by AUSTRALIAN CATHOLIC UNIVERSITY · Jun 1, 2025
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
The GLaD Feasibility Study is a research project designed to learn more about how people change their eating habits after starting a specific type of medication called GLP-1 agonists, which are commonly used to help manage obesity and Type 2 diabetes. This study will involve individuals who are planning to begin this medication and are willing to keep track of what they eat, as well as answer questions about their behavior and mental well-being.
To participate in this study, you need to be at least 18 years old and planning to start a GLP-1 agonist medication, such as Ozempic or Saxenda, for the first time. It's important that you haven't used any GLP-1 medications in the past six months. Participants will not only help researchers gather valuable information but will also get a chance to reflect on their dietary choices and health. This study is currently not recruiting participants, but if you meet the criteria, you may be contacted when it starts.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Aged 18+ years old
- • Intending to commence a prescription for a GLP-1 agonist (may be dual agonist, i.e. Ozempic, Trulicity, Monjaro, or Saxenda) medication, with no use in the previous 6 months
- • The primary reason for commencing the medication will be for diabetes or weight management
- • Willing to participate in dietary recall and questionnaires
- Exclusion Criteria:
- • Aged under 18 years,
- • used a GLP-1 agonist medication in the previous 6 months,
- • unwilling or unable to provide dietary recalls
- • non-English speaking.
About Australian Catholic University
Australian Catholic University (ACU) is a distinguished higher education institution dedicated to advancing knowledge and research in the fields of education, health, and social sciences. As a clinical trial sponsor, ACU leverages its academic expertise and commitment to ethical research practices to facilitate innovative studies aimed at improving health outcomes. The university fosters collaboration among researchers, healthcare professionals, and community stakeholders, ensuring that clinical trials are conducted with rigor and integrity while addressing pressing health challenges. Through its research initiatives, ACU aims to contribute to the evidence base that informs clinical practice and policymaking in Australia and beyond.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Fitzroy, Victoria, Australia
Patients applied
Trial Officials
Evelyn B Parr, PhD
Principal Investigator
Australian Catholic University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported