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Clinical Trials/NCT02888782
NCT02888782
Terminated
Not Applicable

Optimizing Medication Therapy Outcomes for Complex Patients Transitioning From Acute to Primary Care

Memorial University of Newfoundland2 sites in 1 country89 target enrollmentDecember 8, 2016
ConditionsChronic Disease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Disease
Sponsor
Memorial University of Newfoundland
Enrollment
89
Locations
2
Primary Endpoint
Composite Hospital Utilization Rate
Status
Terminated
Last Updated
7 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
December 8, 2016
End Date
June 29, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Deborah Kelly

Associate Professor and Special Advisor of Innovation

Memorial University of Newfoundland

Eligibility Criteria

Inclusion Criteria

  • 50 years of age or older
  • Admitted to a General Medicine ward
  • Take 5 or more chronic medications

Exclusion Criteria

  • Discharge to a long term care facility
  • Life expectancy less than 3 months
  • Have entered palliative care
  • Cognitive impairment (unless a responsible caregiver can provide consent and assist in participation)
  • Non-English speaking
  • Unable to provide informed consent

Outcomes

Primary Outcomes

Composite Hospital Utilization Rate

Time Frame: 30 days post discharge

A composite score of hospital readmission rate and ER visits

Secondary Outcomes

  • Frequency of Family Physician Visits(90 days post discharge)
  • Rehospitalization Rate(90 days post discharge)
  • Number of Emergency Room Visits(90 days post discharge)
  • Mortality Rate(90 days post discharge)

Study Sites (2)

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