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Implementation and Evaluation of a Pharmacist-led Diabetes Care Pathway in Alberta Community Pharmacies (D-PATH)

U

University of Alberta

Status

Enrolling

Conditions

Hypertension
Diabetes Mellitus
Hyperlipidaemia

Treatments

Other: Pharmacist-led diabetes care pathway

Study type

Interventional

Funder types

Other

Identifiers

NCT07339852
Pro00145395

Details and patient eligibility

About

As of 2024, nine percent of Albertans are living with Type 2 diabetes, which increases their risk for cardiovascular disease, stroke, blindness, and kidney failure. Unfortunately, less than half of patients have controlled Type 2 diabetes. We are well aware of the factors which lead to worsening diabetes, but need to give people more support to help them manage their diabetes. Pharmacists are respected health care professionals who are often easier to see that doctors and can help people with diabetes to stay as healthy as possible.

This research project aims to see whether a pharmacist service can help improve diabetes management in people with type 2 diabetes compared to usual care from their family physician or nurse practitionner. The potential impact of this project is to empower people with type 2 diabetes to understand their condition, it's management, and to achieve target blood sugar levels, which will ultimately reduce the risk of diabetes-related complications.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Individuals aged 18 years or older.
  2. Individuals with type 2 diabetes.
  3. Individuals with type 2 diabetes not reaching HbA1c target of under 7.0%

Exclusion criteria

  1. Individuals with type 1 diabetes, gestational diabetes, or other forms of diabetes that are not type 2 diabetes.
  2. Pregnant individuals.
  3. Individuals at their HbA1c target (HbA1c under 7.0%) or those with a limited life expectancy, frailty, or lack hypoglycemic awareness (i.e., those with an A1c target above 7.0%) .
  4. Individuals unable to provide consent or who are unwilling to attend follow-up visits.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

600 participants in 2 patient groups

Pharmacist-led care pathway
Experimental group
Description:
Participants in the intervention arm will receive the care using a shared decision-making pharmacist care pathway approach designed to guide type 2 diabetes management to achieve target A1C levels and reduce the risk of diabetes-related complications. The pharmacist care pathway is modelled after the Canadian Diabetes Association Guidelines. This pathway (tool) will be built into a computer web-based program and include step-by-step, algorithm-guided patient assessment to achieve target A1C levels and reduce the risk of diabetes-related complications. This will occur through follow-ups every 6 weeks for six months duration.
Treatment:
Other: Pharmacist-led diabetes care pathway
Usual Care
No Intervention group
Description:
The control group will involve facilitated relay of information to participants' family physician or nurse practitioner. Participants in the control group will have their pharmacist collect information informing the patient's current diabetes control. Participants will then be given a letter that contains their A1C value, and they will be advised to present it to their family physician or nurse practitioner. No specific suggestions for diabetes management will be detailed in the letter. In the case where the patient does not have a family physician or nurse practitioner, they will be referred to a physician walk-in clinic. A follow-up appointment will be booked for all participants in the control group at 3-months to discuss dietary and lifestyle interventions in the management of type 2 diabetes to maintain participant interest in the study and again at 6-months' time for a final visit.

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Stephanie Gysel, BScPharm, PharmD; Ross Tsuyuki, BScPharm, PharmD, MSc

Data sourced from clinicaltrials.gov

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