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Reorganizing the approach to diabetes through the application of registries

Reorganizing the Approach to Diabetes through the Application of Registries: a non-randomized cross-over trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14359671
Enrollment
800
Registered
2016-10-07
Start date
2015-01-01
Completion date
Unknown
Last updated
2021-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes Nutritional, Metabolic, Endocrine Type 2 diabetes mellitus

Interventions

This is a modified stepped-wedge controlled implementation trial. It's a cross-over design, whereby each community serves as its own control before 'switching' to the intervention at different time po
and, a centralized care coordinator (CC). The CARE platform was designed by OKAKI Health Intelligence Inc. to meet the specific requirements of nursing-driven health programs currently being delivered

Sponsors

University of Alberta
Lead Sponsor
Alliance for Canadian Health Outcomes Research in Diabetes (ACHORD)
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients >18 years of age diagnosed with type 2 diabetes 2. Recently (within last 1-2 years) received care from the First Nations health facility 3. Provided verbal consent for First Nations health care workers to manage their diabetes

Exclusion criteria

Exclusion criteria: 1. Patients with type 1 diabetes 2. Patients <18 years of age 3. Those who are subsequently discovered not to have type 2 diabetes (and were not initially in the baseline period) 4. Those refusing care within the First Nations health facility; patients with type 2 diabetes identified after the conclusion of the baseline phase of the project

Design outcomes

Primary

MeasureTime frame
1. A1c 2. Blood pressure 3. Cholesterol Data collected for regular clinical care is used to assess the primary and secondary outcomes. There is no additional data collected from patients specific to the RADAR study. It may be considered a type of chart review. Timepoints: baseline, end of Intervention (minimum 1 year, depending on the community).

Secondary

MeasureTime frame
1. The proportion of clinical measures and tasks completed in accordance with Canadian Diabetes Association Clinical Practice guidelines (e.g., A1c, BP, cholesterol, foot and eye examination, receipt of vaccinations, smoking cessation counseling) 2. The number of patients registered in CARE 3. The proportion of patients linked to a health services provider Data collected for regular clinical care is used to assess the primary and secondary outcomes. There is no additional data collected from patients specific to the RADAR study. It may be considered a type of chart review. Timepoints: baseline, end of Intervention (minimum 1 year, depending on the community).

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 11, 2026