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NCT05859555

Multimodal Educative Data Feedback for Deprescribing BZD and Related Drugs in Outpatients: a Cluster RCT

Completed NA Last updated 29 November 2024
What this trial tests

NA trial testing Thematic quality circles - Deprescription in Deprescription in 300 participants. Completed in 21 June 2024.

Timeline
5 December 2022
Primary endpoint
21 May 2024
21 June 2024

Quick facts

Lead sponsorRéseau de soins Delta
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment300
Start date5 December 2022
Primary completion21 May 2024
Estimated completion21 June 2024
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Réseau de soins Delta

Who can join

18 and older, any sex, with Deprescription or Benzodiazepine (BZD) and Related Drugs. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Benzodiazepine (BZD) and related drugs are sedative anxiolytics and hypnotics that should be avoided especially in people aged 65 years and older, given the high risk of falling, fracture, dependence, respiratory depression and cognitive disorders. Despite these contraindications, their consumption continues to increase in Switzerland. Although it can be assumed that deprescribing a drug has a direct benefit, it is nevertheless necessary to determine how to implement this process effectively and safely. To change healthcare professionals' prescribing behaviours for BZD, the most common deprescribing interventions include identification of appropriate patients, education and training of GPs and patients, and gradual and appropriate reduction of the dose of BZD. Thus, the DELTA CARE NETWORK and the DELTA VAUD CARE NETWORK have set themselves the task of evaluating the effectiveness of a multimodal deprescribing intervention for Delta primary care physicians and their patients aged 65 and over, in the cantons of Geneva and Vaud. The goal is to reduce the total BZD prescription rate among this population. This quality development project is fully in line with the Quality Federal Commission's objectives of efficiency, safety, patient-centred and in the interests of the patient.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Réseau de soins Delta trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing