Optimizing Medication Therapy for Patients Recently Discharged From Hospital

NCT ID: NCT02888782

Last Updated: 2018-10-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

89 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-08

Study Completion Date

2018-06-29

Brief Summary

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Patients who are discharged from hospital can be overwhelmed when they suddenly have to manage new conditions or medications. These changes can be particularly difficult for people on many medications or with multiple health conditions. There is a real risk that this will lead to emergency room visits, hospital readmission, and even death. In addition to endangering patients, these adverse events are very costly to the healthcare system. The good news is that these events can be preventable if patients receive care that is better coordinated.

Patient-oriented research will be conducted to determine if a pharmacist-led medication therapy management service can improve health outcomes of 'medically complex' patients transitioning from acute to primary care in Newfoundland and Labrador (NL). This a more comprehensive service than their community pharmacist would normally provide. The program will use a new Pharmacist Clinic service to provide care and support which does not currently exist for patients in NL after they leave hospital. After discharge, patients will be randomly divided into two groups: one group will receive care as usual from their doctor; the other group will have their medications assessed by a clinic pharmacist within one week of hospital discharge along with their usual care from their doctor. The two groups will be compared to determine whether specialized pharmacist services after hospital discharge is satisfactory to patients/providers, improves patient health, and reduces emergency room visits, hospital readmissions, and repeat trips to the doctor. If successful, this project will help ensure that patients are taking the right medications in the right way, improving individual health and making better use of healthcare system resources.

Detailed Description

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Conditions

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Chronic Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Pharmacist Consultation

Meet with pharmacist for consultation in addition to regular physician follow up

Group Type EXPERIMENTAL

Pharmacist Consultation

Intervention Type OTHER

Control

Receive regular physician follow up

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Pharmacist Consultation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. 50 years of age or older
2. Admitted to a General Medicine ward
3. Take 5 or more chronic medications

Exclusion Criteria

1. Discharge to a long term care facility
2. Life expectancy less than 3 months
3. Have entered palliative care
4. Cognitive impairment (unless a responsible caregiver can provide consent and assist in participation)
5. Non-English speaking
6. Unable to provide informed consent
Minimum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Memorial University of Newfoundland

OTHER

Sponsor Role lead

Responsible Party

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Deborah Kelly

Associate Professor and Special Advisor of Innovation

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Deborah Kelly, PharmD

Role: PRINCIPAL_INVESTIGATOR

Memorial Univeristy of Newfoundland

Locations

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Health Sciences Center

St. John's, Newfoundland and Labrador, Canada

Site Status

St. Clares Mercy Hospital

St. John's, Newfoundland and Labrador, Canada

Site Status

Countries

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Canada

Other Identifiers

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HREB-2016.221

Identifier Type: -

Identifier Source: org_study_id

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