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Not yet recruiting NCT07102498

A Comparison of Different Units for Blood Glucose (mmol/L and mg/dl) and Hemoglobin A1c (% and mmol/Mol) Results.

No phase Interventional Diabetes

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: BG mmol/L, BG mg/dl, A1c percent, A1c mmol/mol.
Who it may be relevant to
Registry conditions: Diabetes. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Comparison of Units Used for Blood Glucose and HbA1c Testing

Overview

A comparison of people's reactions to hypothetical test results using different units.

Detailed description

Comparing how people respond to hypothetical blood glucose results in mg/dl units versus mmol/L units, and also how they respond to hypothetical HbA1c results in % units versus mmol/mol units.

Interventions

  • Behavioral BG mmol/L
    BG presented in mmol/L (the standard presentation in Canada)
  • Behavioral BG mg/dl
    BG presented in mg/dl
  • Behavioral A1c percent
    HbA1c presented in percent (the standard presentation in Canada)
  • Behavioral A1c mmol/mol
    HbA1c presented in mmol/mol

Primary outcome measures

  • Opinion about result [Time frame: Immediately after the intervention]

Eligibility criteria

Inclusion criteria

  • Able to use a computer
  • Able to use the internet
  • Able to read and respond to questions in English or French
  • Adults 18+ years old living in Canada

Exclusion criteria

\- Not meeting inclusion criteria

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Factorial
Masking
Single blind
Primary purpose
Health services research

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07102498 · units

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗