Type 2 Diabetes Clinical Trial
Official title:
Patients and Care Providers Perspectives and Experience With Decision Aid Tool for Self-monitoring of Blood Glucose
Putting the limited use of titration algorithms in the context of escalating diabetes prevalence rates, strategies and tools are urgently needed to help both patients and primary care providers efficiently initiate and continue basal insulin therapy. Basel insulin is considered to be the appropriate strategy after oral diabetic agent failure. This project could set the stage for the need for a blood glucose meter with built-in algorithms designed to support decision making by patients as well as care providers. Furthermore, the project will evaluate the uptake and use of the newly developed Meter by Abbott Diabetes Care, which was launched in Canada in October 2014, and its impact on primary care diabetes consultation.
The objectives of this study are to
1. Describe patients' and care providers' satisfaction associated with the use of the
FreeStyle Precision Neo-Meter
2. Evaluate the uptake and use of the Meter
3. Describe the impact of the Meter on primary care diabetes consultation from care
providers' perspectives.
In order to achieve the objectives of this study, diabetes healthcare providers and people
with type 2 diabetes who have been using the Neo meter will be interviewed. Maximum
variability will be sought for provider discipline and patient demographic characteristics.
Sampling will continue until theme saturation is reached. A total of up to 20 (10 care
providers and 10 people with diabetes) will be interviewed for this study.
Diabetes healthcare provider interview: Two care providers from each discipline including
physicians, nurses, nurse educators and dietitians in Southwestern Ontario, Canada, who have
been using the Neo meter will be recruited for interviews. Care providers satisfaction will
be assessed after the use of the Meter with sample representation of sole and team based
practices.
Patient interviews: Eligible patients who agreed to participate in the study will be
provided with a Neo meter and test strips. Their care providers will provide them with
instructions, guidance and support in using the device as part of their self-management
activities. Patients will be interviewed 3 months after (post only) the use of the Meter to
assess their satisfaction with its functionality, capacity, design and ease-of-use.
Interviews will take place at a location and time convenient for participants and will take
approximately 45min-60min in Oct/Nov 2015. Interviews will be audio tape recorded to allow
for a fluid discussion such that the interviewer does not need to stop the conversation to
take notes. A letter of information and consent form will be provided to participants.
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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