NCT04142645

Brief Summary

Pilot study of the OptiMEDs intervention: a complex intervention for multidisciplinary medication review (including nurses, pharmacists, and physicians) in nursing homes (NH), with ICT-support for the evaluation of the appropriateness of prescribing and for side-effect monitoring.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
148

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2019

Shorter than P25 for not_applicable

Geographic Reach
1 country

3 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 30, 2019

Completed
9 days until next milestone

Study Start

First participant enrolled

October 9, 2019

Completed
20 days until next milestone

First Posted

Study publicly available on registry

October 29, 2019

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 20, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 20, 2020

Completed
Last Updated

November 29, 2021

Status Verified

November 1, 2021

Enrollment Period

5 months

First QC Date

September 30, 2019

Last Update Submit

November 25, 2021

Conditions

Keywords

Medication ReconciliationAged

Outcome Measures

Primary Outcomes (9)

  • Software/user problems

    monthly number of interventions for software/user problems (n)

    6 months

  • functionality problems

    Number of functionality problems (n)

    6 months

  • workload

    Timing of workload for nurses \& pharmacists regarding the use of OptiMEDs (time)

    6 months

  • medication chart review

    duration of a medication chart review by GP and nurse (time)

    6 months

  • practical problems

    listing of practical problems for organizing the medication chart review

    6 months

  • GPs that refuse

    number of GPs that refuse to participate / accept to participate (n)

    6 months

  • non-consenting eligible residents (n)

    Number of non-consenting eligible residents legally capable to give consent (n)

    6 months

  • Non-consenting proxies for eligible residents (n)

    Number of non-consenting proxies for eligible residents legally not capable to give consent

    6 months

  • Optimeds completion

    Number of symptom observations and medication reviews completed (on time) (n)

    6 months

Secondary Outcomes (9)

  • number of medications

    4 months

  • number of anticholinergics

    4 months

  • number of candidates for de-prescribing

    4 months

  • patient-related pain

    4 months

  • patient-related alertness

    4 months

  • +4 more secondary outcomes

Study Arms (2)

Intervention

EXPERIMENTAL

The intervention group (i.e. all eligible and consented residents of 2 NHs) will receive the OptiMEDs intervention: the combination of an electronic decision support tool (for the appraisal of potentially inappropriate medication use, anticholinergic use, or medications that can be de-prescribed in view of limited life expectancy) with focused nurse observations (using a list of potential medication-related symptoms based on the individual medication chart of the nursing home residents), that will serve as the basis during a multidisciplinary medication review with the input of GPs, trained community pharmacists and nurses.

Device: OptiMEDs

Control

NO INTERVENTION

The control group (i.e. all eligible and consented residents of one control NH) will receive usual care .

Interventions

OptiMEDsDEVICE

The OptiMEDs intervention is a multi-faceted intervention combining: 1. an ICT platform: * automatic and secure capture of individual prescribing information from the electronic medication administration records in the nursing home * a tool for structured nurse observations of side effects, derived from the existing Pharmanurse application (20) (used to list potential medication side effects, based on the individual medication chart of the nursing home residents) to support monitoring of medication safety by nurses. * an electronic decision support tool for the appraisal of potentially inappropriate medication (explicit criteria of misuse and underused of medication, based on existing lists of explicit criteria (PIMs)), use of medication with anticholinergic properties and medication inappropriate in view of the limited life expectancy. 2. a multidisciplinary medication review with the input of GPs, trained community-pharmacists and nurses.

Intervention

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

You may qualify if:

  • located in East Flanders
  • size: \> 100 beds
  • mixed population of high care dependent and low care-dependent residents with and without dementia
  • software of Care Solutions or Farmad is used for electronic handling of the medication chart
  • the NH management as well as the responsible CRA and the community pharmacist who delivers the medication in the NH give their written agreement to participate
  • aged 65 years or older
  • mentally fit as well as cognitive impaired NH residents will be included after Informed Consent given by the resident (mentally capable residents) or his representative (cognitive impaired residents, defined as a sumscore of 6 or more on the KATZ items of disorientation in time and place).

You may not qualify if:

  • they have a limited life-expectancy (less than 3 months, as judged and documented by the treating GP)
  • they are residing in a short-stay / revalidation bed
  • GP refused to have his NH residents included in this pilot

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

WZC Sint-Jozef Deinze

Deinze, Oost-Vlaanderen, 9800, Belgium

Location

WZC Sint-Jozef Gent

Ghent, Oost-Vlaanderen, 9000, Belgium

Location

WZC Liberteyt

Ghent, 9000, Belgium

Location

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Study Officials

  • Thierry Christiaens, PhD, MD

    Faculty of Medicine and Health Sciences

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: A pragmatic cluster-randomized trial with the inclusion of two NHs where the feasibility and acceptability of the OptiMEDs intervention will be tested and one NH where the standard of care will be registered.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 30, 2019

First Posted

October 29, 2019

Study Start

October 9, 2019

Primary Completion

March 20, 2020

Study Completion

March 20, 2020

Last Updated

November 29, 2021

Record last verified: 2021-11

Data Sharing

IPD Sharing
Will not share

Locations