Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06888687

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

Led by Australian Catholic University · Updated on 2025-05-23

156

Participants Needed

1

Research Sites

80 weeks

Total Duration

On this page

Sponsors

A

Australian Catholic University

Lead Sponsor

A

Abbott Diabetes Care

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or older
  • Living anywhere in Australia with a postal address
  • Diagnosed with type 2 diabetes by a GP or endocrinologist
  • Current HbA1c level of 7.0% or higher
  • Have a smartphone and able to use it independently
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Using insulin therapy within the last three months or medications affecting blood glucose (e.g., steroids)
  • Used continuous glucose monitoring within the last six months
  • High score on Eating Disorder Examination Questionnaire (EDE-Q) indicating eating disorder risk
  • Currently or recently (within three months) consulting with an Accredited Practicing Dietitian
  • Not weight stable (more than 5 kg change in last three months)
  • Experienced severe hypoglycaemic event requiring assistance in last six months
  • Changed antihyperglycaemic medications within last three months
  • Pregnant or breastfeeding within 24 weeks
  • History of psychotic or major psychiatric disorders
  • History of blood disorders affecting HbA1c outcomes (e.g., anemia, thalassemia)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Australian Catholic University

Melbourne, Victoria, Australia, 3065

Actively Recruiting

Loading map...

Research Team

E

Evelyn B Parr, PhD

CONTACT

K

Katherine Roberts-Thomson, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

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