Insulin Initiation and Adherence Behaviours: a Cross Sectional Survey of Indian HCPs & Patients With Type 2 Diabetes
- Conditions
- Type 2 Diabetes
- Interventions
- Other: No treatment given
- Registration Number
- NCT06517784
- Lead Sponsor
- Novo Nordisk A/S
- Brief Summary
This is a cross-sectional study planned among patients with Type 2 Diabetes (T2D) and Health Care Providers (HCPs) who treat T2D patients. Study participants will be recruited through existing databases/panels to complete a 30-minute self-administered online survey. The purpose of the study is to understand the insulinization barriers and the insulin adherence behaviours of both HCPs and patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 752
For patients
- 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 to 18 years at the time of signing informed consent.
- Diagnosed with T2D
- Currently seeing an HCP for T2D
- Initiated on insulin within the past 12 months
- Prescribed insulin on a permanent basis
- Currently taking insulin via a vial and syringe or insulin pen
For HCP
- 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 to 18 years at the time of signing informed consent.
- Primary care physician (PCP) with degree in internal medicine or general medicine, diabetologist with degree in internal medicine or general medicine plus diploma in diabetology, or endocrinologist
- Has been in practice a minimum of 2 years
- Diabetologist/endocrinologist: treats at least 50 T2D patients per month
- PCP: treats at least 40 T2D patients per month
- Currently initiates T2D patients on insulin
- Treats 20 percent or more of T2D patients with insulin
- 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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Health care providers No treatment given Health care providers who treat patients with type 2 diabetes Patients No treatment given Patients with type 2 diabetes
- Primary Outcome Measures
Name Time Method The barriers toward insulin initiation among HCPs & patients At time of data abstraction (Day 1) Barriers to insulin initiation = Likert scale: 1=Strongly disagree, 5=Strongly agree
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Novo Nordisk India
🇮🇳Bangalore, India