Skip to main content
Clinical Trials/NCT01504672
NCT01504672
Completed
N/A

A Randomized Controlled Pharmacist Intervention Study to Reduce Drug-related Problems and Readmissions Among Old People With Dementia

Umeå University2 sites in 1 country460 target enrollmentJanuary 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cognitive Impairment
Sponsor
Umeå University
Enrollment
460
Locations
2
Primary Endpoint
Number of Patients Readmitted Because of Drug Related Reasons
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The aim of this randomized controlled study is to investigate if medication reviews performed by a clinical pharmacist as part of a ward team can reduce drug related problems and reduce readmissions to hospital among elderly patients (≥65 years) with dementia and cognitive failure.

Four hundred and sixty patients will be recruited and randomized to control (usual care) and intervention group (enhanced service in which a pharmacist is part of the health care team).

Six months after the last patient of the 460 has been discharged the study will be closed. Data about the number of readmissions and visits to the emergency room will be collected during the six-month follow-up and also, the costs associated with each visit or admission. Time until institutionalization will be compared between intervention group and control group.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
August 2015
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hugo Lovheim

Principal Investigator

Umeå University

Eligibility Criteria

Inclusion Criteria

  • Patients with dementia or cognitive impairment
  • Patients ≥ 65 years

Exclusion Criteria

  • Patients previously admitted to the study wards during the study period

Outcomes

Primary Outcomes

Number of Patients Readmitted Because of Drug Related Reasons

Time Frame: Six months follow-up

Secondary Outcomes

  • Frequency of Emergency Department Visits During the 6-month Follow-up.(Six months follow-up)
  • Change in the Number of Participants With Potentially Inappropriate Medications, According to the Swedish National Board of Health and Welfare, at Admission and Discharge Between Intervention and Control Group(Index admission (at randomization) and index discharge (duration of index admission, mean days 8.7))
  • Cost for Visits for Readmissions and to the Emergency Department Compared Between Patients in the Control Group and Intervention Group.(Six months follow-up)
  • Number of Participants Institutionalized After Discharge, in Control Group and Intervention Group.(Six months follow-up)

Study Sites (2)

Loading locations...

Similar Trials