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Recruiting NCT06888687

Comparison of Dietetics Support With and Without Continuous Glucose Monitoring in Individuals With Type 2 Diabetes.

Trial Parameters

Condition Type 2 Diabetes Mellitus (T2DM)
Sponsor Australian Catholic University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 156
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-05-12
Completion 2026-11-28
Interventions
Dietetic supportContinuous glucose monitoring

Brief Summary

A parallel, single-blinded, randomised clinical trial conducted remotely across Australia from the Mary MacKillop Institute for Health Research (MMIHR, Australian Catholic University) for individuals with type 2 diabetes, by researchers from Australian Catholic University, University of Adelaide, University of Queensland, University of Wollongong, Monash University, Monash Partners, Deakin University, La Trobe University and Melbourne University.

Eligibility Criteria

Inclusion Criteria: * Aged 18+ years * Reside anywhere in Australia and have a postal address * Confirmed T2D diagnosis by a GP/endocrinologist * Current HbA1c of ≥7.0% * Have a smartphone and able to independently use it Exclusion Criteria: * Under the age of 18 years * Use of insulin therapy (within the last three months) or medications which interfere with blood glucose levels (i.e. steroids) * Use of CGM within the last six months * Eating Disorder Examination Questionnaire (EDE-Q) global score \>2.8 OR global score \> or equal to 1.52, with sum of Q14-18 \> or equal to 4 * Currently having ongoing consultations with an APD or have had a consult with an APD (within last three months) * Not weight stable (\>5 kg change over last three months) * Severe hypoglycaemic event (i.e. requiring assistance) within last six months * Change of antihyperglcyaemic medications within last three months * Women who are pregnant or breastfeeding (within 24 weeks) * History of psychotic disorder, or

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