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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02963636
Other study ID # 106238
Secondary ID
Status Completed
Phase N/A
First received February 17, 2016
Last updated November 14, 2016
Start date August 2015
Est. completion date April 2016

Study information

Verified date November 2016
Source Laval University
Contact n/a
Is FDA regulated No
Health authority Canada: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The project objective is to evaluate the impact of the recent addition of pharmacists within family medicine groups (FMGs) on organizational and clinical parameters. The process by which changes occur and the level of pharmacists' activities will also be assessed. The ultimate goal of the project is the development of an accompanying guide to facilitate the work of the pharmacist in monitoring complex patients in primary care medical clinics.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Willing to meet with the pharmacist and;

- Consuming drugs of four or more different pharmacological classes or having to take at least four doses per day and;

- aged 70 or over with at least two criteria of vulnerability or aged less than 70 with at least 3 criteria of vulnerability or had a recent loss of autonomy or in post- hospitalization with medication changes in the hospital.

Exclusion Criteria:

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Pharmacist clinical intervention
Pharmacists will make a clinical intervention with patients. They will review patient drug therapy already prescribed in their usual care. This includes a medication reconciliation, an assessment of drug related problems, an assessment of the regimen complexity and adherence to treatment. A care plan will be elaborated. Moreover, immediate and future interventions with the patient or other health professionals will be implemented and monitored. There will be no drug or devices tested, it is a human clinical intervention by a pharmacist.

Locations

Country Name City State
Canada CIUSSS de la Capitale-Nationale Québec Quebec

Sponsors (4)

Lead Sponsor Collaborator
Laval University Fonds de la Recherche en Santé du Québec, McGill University, Université de Sherbrooke

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of drug related problems 3 to 6 months No
Secondary Regimen complexity Medication regimen complexity index (MRCI) 3 to 6 months No
Secondary Medication adherence Proportion of days covered (PDC) 3 to 6 months No
Secondary Quality of care provided by the clinical team (pharmacists, doctors, nurses, etc.) Quality indicators (proposed by INESSS) 3 to 6 months No
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