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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05737810
Other study ID # DAS-7687
Secondary ID U1111-1286-0886
Status Completed
Phase
First received
Last updated
Start date March 27, 2023
Est. completion date April 17, 2023

Study information

Verified date May 2023
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The main purpose of this study is to explore experiences and understand the unmet needs of people with Type 2 Diabetes (T2D) among those who are being managed with basal insulin and those who are insulin naïve in order to understand perspectives for a once weekly insulin option; including any potential barriers to being managed with insulin therapy overall. Study participants will be recruited to complete a 15-minute self-administered online survey.


Recruitment information / eligibility

Status Completed
Enrollment 700
Est. completion date April 17, 2023
Est. primary completion date April 17, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Informed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol). 2. Male or female, age above or equal between 18 to 65 years at the time of signing informed consent. 3. Diagnosed with T2D and currently treating T2D with at least one medication 4. Insulin user that is not using insulin pump 5. Lives in a target country Exclusion Criteria: 1. Previous participation in this study. Participation is defined as having given informed consent in this study 2. Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation 3. Does not meet inclusion criteria requirements

Study Design


Intervention

Other:
No treatment given
No treatment given

Locations

Country Name City State
Australia Novo Nordisk Investigational Site Sydney
France Novo Nordisk Investigational Site Chartres
India Novo Nordisk Investigational Site Bengaluru
Korea, Republic of Novo Nordisk Investigational Site Seoul
Mexico Novo Nordisk Investigational Site Mexico City
Saudi Arabia Novo Nordisk Investigational Site Riyadh
United Kingdom Novo Nordisk Investigational Site London

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Countries where clinical trial is conducted

Australia,  France,  India,  Korea, Republic of,  Mexico,  Saudi Arabia,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Current medication burden Numerical; Multiple select from defined list At the time of survey response (Day1)
Primary Injection perceptions Likert scale for measurement of agreement from 1 "strongly disagree" to 7 "strongly agree" At the time of survey response (Day1)
Primary Attitudes regarding T2D overall Likert scale for measurement of agreement from 1 "strongly disagree" to 7 "strongly agree" At the time of survey response (Day1)
Primary Attitudes regarding T2D treatment Likert scales for measurement of satisfaction from 1 "extremely unsatisfied" to 7 "extremely satisfied" and agreement from 1 "strongly disagree" to 7 "strongly agree" At the time of survey response (Day1)
Primary Attitudes regarding insulin icodec Likert scales for measurement of likelihood from 0 "not at all likely" to 10" extremely likely" and agreement from 1 "strongly disagree" to 7 "strongly agree; Rank top 3 from defined list At the time of survey response (Day1)
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