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Clinical Trials/NCT03369652
NCT03369652CompletedNot Applicable

Can Telephone Contact After Discharge Between Geriatrician, Clinical Pharmacist and General Practitioner About Medication Review in Hospital Improve the Medication in Older Patients? A Feasibility Study.

Odense University Hospital3 sites in 1 country232 target enrollmentStarted: November 24, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
232
Locations
3
Primary Endpoint
Parts of the intervention completed

Study Overview

Brief Summary

In this trial, the feasibility of cooperation between clinical pharmacists and physicians by conducting a telephone follow-up conversation between the hospital geriatrician, the general practitioner and the clinical pharmacist is evaluated. During hospital stay the clinical pharmacist and the geriatrician will review older patients' medication and discuss the future treatment with the general practitioner after discharge by telephone or medico-technology.

The first part of the feasibility study will be a qualitative baseline measure of characteristics of the participants and work flow. The second part will be a pilot randomized controlled study where participants will be allocated to either usual care or medication review and follow up contact

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • * 5 drugs or more

Exclusion Criteria

  • Terminal illness
  • Not able to speak and understand Danish

Arms & Interventions

Intervention

Experimental

Medication history by pharmaconomist. Medication review by pharmacist, patient interview, and conference with physician in hospital, telephone contact to general practitioner after discharge, medication report sent to primary care.

Intervention: Medication review (Behavioral)

Control

No Intervention

Medication history by pharmaconomist. Usual care by physicians.

Outcomes

Primary Outcomes

Parts of the intervention completed

Time Frame: Day 1 after discharge

In the intervention Group only, it is measured, how many of the elements of the intervention the patient actually have received

Changes in number of medications

Time Frame: At admission and at discharge

Increase or decrease in number of medications from admission to discharge

Changes in the Electronic Medication Profile (FMK)

Time Frame: 14 days after discharge

How many changes have been Applied to the Electronic Medication Profile

Secondary Outcomes

  • Changes in patient-experienced quality of life(At admission and 14 days after discharge)
  • Number of readmissions(within 30 days after discharge)
  • Number of visits at general practitioner(within 30 days after discharge)
  • Number of emergency visits(within 30 days after discharge)
  • Patient satisfaction with the discharge(14 days after discharge)
  • Health care professionals satisfaction(3 months after implementation)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lene V. Ravn-Nielsen

Pharmacist

Odense University Hospital

Study Sites (3)

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