Diabetes Clinical Trial
Official title:
A Collaborative Care Model for Chronic Disease Management in Diabetes - Involvement of Community Pharmacists in Complex Care Plans, a Pilot Study
| NCT number | NCT02399332 |
| Other study ID # | REB15-0673 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | March 2016 |
| Est. completion date | December 2017 |
| Verified date | May 2019 |
| Source | University of Calgary |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This project is an initiative to bring physicians, nurses, community pharmacists and patients together in collaborative planning in the management of diabetes, which aligns with the collaborative, team based aspects of family medicine as a community based discipline. Alberta funds both physicians and community pharmacists to complete a comprehensive assessment and plan for patients with qualifying medical conditions. Our research hypothesis is that a collaborative approach between healthcare providers involved in delivering care will improve individual patient outcomes with the primary outcome being improved glycemic control. Health care utilization and medication adherence will also be assessed. This project will compare the results of comprehensive annual health care plans implemented over a period of twelve months with or without involvement from community pharmacists. It is hypothesized that involvement of community pharmacists and their collaboration with physicians will lead to improved outcomes.
| Status | Completed |
| Enrollment | 16 |
| Est. completion date | December 2017 |
| Est. primary completion date | December 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Age = 18 - Patients who have diabetes with HbA1C over target (>7) and who qualify for a complex care plan completion. Exclusion Criteria: - Pregnancy - Unwilling to participate/provide written consent - Unable or unwilling to participate in planned follow-ups |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| University of Calgary |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in HbA1C from baseline at one year | 1 year | ||
| Secondary | Change in systolic BP from baseline at one year | 1 year | ||
| Secondary | Change in diastolic BP from baseline at one year | 1 year | ||
| Secondary | Change in Low Density Lipoprotein (LDL) from baseline at one year | 1 year | ||
| Secondary | Change in weight from baseline at one year | 1 year | ||
| Secondary | Change in BMI from baseline at one year | 1 year | ||
| Secondary | Change in hospital admissions from baseline at one year | 1 year | ||
| Secondary | Change in family physician visits from baseline at one year | 1 year | ||
| Secondary | Change in emergency room visits from baseline at one year | 1 year | ||
| Secondary | Change in medication adherence from baseline at one year | 1 year |
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