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Patient Preference Study in Type-2 Diabetes Mellitus: Discrete Choice Experiment (DCE) to Support Novo Nordisk's Long-Acting Insulin

Patient Preference Study in Type-2 Diabetes Mellitus: Discrete Choice Experiment (DCE) to Support Novo Nordisk's Long-Acting Insulin

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06592950
Acronym
DCE
Enrollment
513
Registered
2024-09-19
Start date
2023-11-02
Completion date
2024-04-29
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type-2 Diabetes Mellitus (T2DM)

Brief summary

The primary objective of this research is to assess T2DM patient preferences for a once weekly insulin treatment. The study involves a qualitative interview phase and quantitative survey phase with a Discrete Choice Experiment (DCE).

Interventions

OTHERNo treatment given

Online survey

Sponsors

Novo Nordisk A/S
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient is an adult aged 18 years or over * Patient was diagnosed with type-2 diabetes mellitus (T2DM) greater than or equal to 180 days prior to the day of screening * Patient is currently prescribed a diabetes treatment (e.g., Metformin/Sus, DPP4i, SGLT2i, GLP-1 RA and/or basal insulin) * Patient is willing and able to provide written informed consent to participate For qualitative interviews: * Patient is a fluent speaker of English and is able to read, write, and fully understand the English language * Patient is a resident in Canada For quantitative online survey: * Patient is a fluent speaker of the local language (English/French/Spanish or Japanese) and is able to read, write and fully understand the local language * Patient is a resident of either Canada, France, Spain or Japan

Exclusion criteria

* Patient is currently employing a basal-bolus insulin treatment regimen to manage their diabetes * Patient is unwilling or unable to comply with the needs of the study or has a physical, behavioural or mental condition that, in the opinion of the recruiter may affect the patient's ability to take part in the study, understand the nature, scope and possible consequences of the study, or the responses they might provide.

Design outcomes

Primary

MeasureTime frameDescription
T2DM patient preferences for a once weekly insulin treatmentDay of interview/survey completion (Day 1)Pre-defined open-ended questions and Discrete Choice Experiment online survey

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026