Eliminating Risk of Preventable Adverse Drug Events at the Hospital-community Interface of Care

NCT ID: NCT01164137

Last Updated: 2013-02-15

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

156 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-11-30

Study Completion Date

2013-02-28

Brief Summary

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This initiative aims to decrease the risk of medication errors at the hospital-community interface as well as health system utilization following hospital discharge by implementing a pharmacist-led medication reconciliation in the patients' home within 72 hours of hospital discharge.

Detailed Description

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The goals of this initiative are to decrease the risk for medication errors at the hospital community interface of care, thus decreasing preventable adverse drug events and preventable drug-related health system utilization following hospital discharge. This initiative has four objectives that aim to:

1. Develop and test a community-based medication reconciliation process/intervention.
2. Design and conduct a randomized controlled trial to examine the impact of the intervention on post-discharge health services utilization by comparing a set of outcome variables between intervention and non-intervention groups.
3. Design a risk prediction model that helps identify patients discharged from in-patient care with the highest level of need for the intervention.
4. Determine whether a community-based medication reconciliation process/intervention adds risk reduction value to individuals who have undergone an in-hospital medication reconciliation.

Conditions

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Adverse Drug Events

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Medication Reconciliation Intervention

Participants receiving a pharmacist-led home intervention conducted within 72 hours of hospital discharge aimed at identifying and correcting medication discrepancies.

Group Type EXPERIMENTAL

Medication Reconciliation

Intervention Type BEHAVIORAL

A pharmacist-led home intervention conducted within 72 hours of hospital discharge aimed at correcting and identifying medication discrepancies.

Medication Reconciliation Non-Interven.

Participants not receiving a pharmacist-led home intervention conducted within 72 hours of hospital discharge aimed at identifying and correcting medication discrepancies.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Medication Reconciliation

A pharmacist-led home intervention conducted within 72 hours of hospital discharge aimed at correcting and identifying medication discrepancies.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Patients attending the WestView Health Centre Medicine/Family Health Unit with at least one medication at discharge.

Exclusion Criteria

* First Nations persons
* Residents of continuing care or assisted living facilities
* Persons not residing in the Edmonton, AB, Canada region
* Persons who obtain a score of 19 or less on the Mini Mental State Examination (MMSE)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Westview Physician Collaborative

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Allan Bailey, M.D.

Role: PRINCIPAL_INVESTIGATOR

Westview Physician Collaborative

Grace Moe, M.Sc.P.T.

Role: STUDY_DIRECTOR

WestView Primary Care Network

Locations

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WestView Health Centre

Stony Plain, Alberta, Canada

Site Status

Countries

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Canada

Other Identifiers

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CMPA#2026

Identifier Type: -

Identifier Source: org_study_id

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