RecruitingNot ApplicableNCT05842928

Patient-centred Deprescribing of Psychotropic, Sedative and Anticholinergic Medication in Elderly Patients With Polypharmacy

Patient-centred Deprescribing of Psychotropic, Sedative and Anticholinergic Medication in Elderly Patients With Polypharmacy: a Cluster-randomised Trial


Sponsor

Ludwig-Maximilians - University of Munich

Enrollment

352 participants

Start Date

Mar 25, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The PARTNER study is a multicentre, two-arm, pragmatic cluster-randomised trial evaluating the impact of a focused and patient-centred cooperation between general practitioners (GPs) and community pharmacists (PARTNER intervention) on reductions in the use of psychotropic, sedative and anticholinergic potentially inappropriate medication (PSA-PIM) compared to a control intervention. The PARTNER intervention comprises (1) education for health care professionals, (2) an interprofessional workshop and case conference, (3) a pharmacy visit with brown bag/medication review and patient empowerment, (4) GP practice visit with shared decision making. The control intervention only comprises a pharmacy visit with brown bag review.


Eligibility

Min Age: 65 Years

Plain Language Summary

Simplified for easier understanding

Older adults are frequently prescribed multiple medications (polypharmacy), including drugs that affect the brain and nervous system — sleep medications, opioids, antipsychotics, antidepressants, and others. While these can be necessary, they also carry significant risks in elderly patients including falls, cognitive decline, and adverse drug interactions. Deprescribing — carefully and systematically reducing unnecessary medications — can improve health outcomes, but it requires careful coordination between doctors and pharmacists. This study tests a patient-centred deprescribing programme for people aged 65 and older who take 5 or more medications including at least one potentially inappropriate psychotropic/sedative/anticholinergic drug. Participants must be capable of giving consent and have a regular GP and pharmacy. People with terminal illness, severe psychiatric conditions, or inability to participate in questionnaires and appointments are excluded. Polypharmacy in the elderly is a growing patient safety issue as populations age. A structured, collaborative GP-pharmacist approach to safely reducing inappropriate medications could prevent falls, hospitalizations, and cognitive problems — improving both quality and length of life for older adults.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALPARTNER intervention

The PARTNER intervention includes the following components: 1. Education for health care professionals A) written manual on deprescribing PSA-PIM, which consists of brief information and more detailed explanations; B) access to digital instructional videos/podcasts that address potential problems in deprescribing and provide possible solutions; C) checklist for identification of drug-related problems for pharmacists; D) tapering support tool to facilitate the selection of tapering schemes; E) divisibility list for PSA-PIM to support the implementation of tapering schemes; F) empowerment brochures for patients each focussing on one PSA-PIM subgroup 2. Interprofessional workshop and case conference for GPs and pharmacists 3. Pharmacy visit (brown bag/medication review) including patient empowerment 4. GP practice visit including shared decision making (SDM)

BEHAVIORALControl intervention

The control intervention only comprises a pharmacy visit with brown bag review.


Locations(3)

University of Bielefeld

Bielefeld, Germany

University Hospital, LMU Munich

Munich, Germany

Witten/Herdecke University

Witten, Germany

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05842928


Related Trials