Attitudes and Unmet Needs Among Type 2 Diabetes Patients
2 other identifiers
observational
700
7 countries
7
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2023
Shorter than P25 for all trials
7 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 10, 2023
CompletedFirst Posted
Study publicly available on registry
February 21, 2023
CompletedStudy Start
First participant enrolled
March 27, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 17, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
April 17, 2023
CompletedMay 15, 2023
May 1, 2023
21 days
February 10, 2023
May 12, 2023
Conditions
Outcome Measures
Primary Outcomes (5)
Current medication burden
Numerical; Multiple select from defined list
At the time of survey response (Day1)
Injection perceptions
Likert scale for measurement of agreement from 1 "strongly disagree" to 7 "strongly agree"
At the time of survey response (Day1)
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)
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)
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)
Study Arms (1)
People with Type 2 Diabetes
Participants are recruited via email through online panel companies
Interventions
Eligibility Criteria
The main purpose of this study is to explore experiences and understand the unmet needs of people with Type 2 Diabetes 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.
You may qualify if:
- Informed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol).
- Male or female, age above or equal between 18 to 65 years at the time of signing informed consent.
- Diagnosed with T2D and currently treating T2D with at least one medication
- Insulin user that is not using insulin pump
- Lives in a target country
You may not qualify if:
- Previous participation in this study. Participation is defined as having given informed consent in this study
- Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Novo Nordisk A/Slead
Study Sites (7)
Novo Nordisk Investigational Site
Sydney, Australia
Novo Nordisk Investigational Site
Chartres, France
Novo Nordisk Investigational Site
Bengaluru, India
Novo Nordisk Investigational Site
Mexico City, Mexico
Novo Nordisk Investigational Site
Riyadh, Saudi Arabia
Novo Nordisk Investigational Site
Seoul, South Korea
Novo Nordisk Investigational Site
London, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Clinical Transparency (dept. 2834)
Novo Nordisk A/S
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 10, 2023
First Posted
February 21, 2023
Study Start
March 27, 2023
Primary Completion
April 17, 2023
Study Completion
April 17, 2023
Last Updated
May 15, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will share
"According to the Novo Nordisk disclosure commitment on novonordisk-trials.com"