Skip to main content
Clinical Trials/NCT06470308
NCT06470308
Active, Not Recruiting
N/A

Prescribing Outcomes of a General Practitioner-Targeted Deprescribing Educational Intervention in Older Adults With Polypharmacy: A Cluster Randomized Trial

University of Crete1 site in 1 country200 target enrollmentNovember 18, 2024

Overview

Phase
N/A
Intervention
Control Arm
Conditions
Medication Overuse
Sponsor
University of Crete
Enrollment
200
Locations
1
Primary Endpoint
Potentially Inappropriate Medication
Status
Active, Not Recruiting
Last Updated
2 months ago

Overview

Brief Summary

Polypharmacy is a common and growing public health concern across healthcare settings worldwide and is associated with an increased risk of inappropriate prescribing and adverse drug events. Deprescribing-defined as the supervised withdrawal of potentially inappropriate medications using structured tools and clinical judgment-has been proposed as a strategy to improve prescribing safety. In Greece, formal initiatives and evidence evaluating deprescribing interventions in primary care remain limited.

This study is a cluster randomized controlled trial evaluating the effect of an educational intervention for general practitioners (GPs) on prescribing safety in primary care. Participating GPs are randomized in an approximately 1:1 ratio to an intervention or control arm. GPs in the intervention arm receive structured education and training on medication review and deprescribing, including the use of validated deprescribing tools such as the Beers Criteria. GPs in the control arm provide usual care and do not receive any educational intervention.

Patients receiving care from participating GPs are recruited, and prescribing outcomes are assessed at the patient level. The primary outcome is change in prescription medications following the intervention, comparing patients cared for by GPs in the intervention arm versus those cared for by GPs in the control arm.

Registry
clinicaltrials.gov
Start Date
November 18, 2024
End Date
March 1, 2026
Last Updated
2 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Alexandros Paraskevopoulos

MD , PhD Candidate

University of Crete

Eligibility Criteria

Inclusion Criteria

  • community-dwelling patients
  • Age ≥ 65 years
  • Receive at least 5 medication ( polypharmacy )

Exclusion Criteria

  • hospitalized or patients living in nursing home
  • Incapable of giving written consent

Arms & Interventions

Control Arm

No educational intervention will be provided to the general practitioners of the selected patients.

Intervention Arm

An educational intervention and training in deprescribing algorithms and deprescribing tools ( Beers Criteria) will be provided to the general practitioners caring for the patients selected in the intervention arm.

Intervention: Medication Reviews and Deprescribing

Outcomes

Primary Outcomes

Potentially Inappropriate Medication

Time Frame: 1 years

Determine if there is reduction in potentially Inappropriate medication after a deprescribing education intervention

Number of medications

Time Frame: 1 year

Determine if there is reduction in number of medications after a deprescribing education intervention

Study Sites (1)

Loading locations...

Similar Trials