NCT03539276

Brief Summary

An education intervention to promote medication reviews and interdisciplinary discussions within long-term care facilities with the aim of improving medication regimen among residents with severe dementia

Trial Health

87
On Track

Trial Health Score

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

Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2014

Geographic Reach
1 country

1 active site

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

Study Start

First participant enrolled

March 1, 2014

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2014

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2015

Completed
2.5 years until next milestone

First Submitted

Initial submission to the registry

May 16, 2018

Completed
13 days until next milestone

First Posted

Study publicly available on registry

May 29, 2018

Completed
Last Updated

June 1, 2018

Status Verified

May 1, 2018

Enrollment Period

7 months

First QC Date

May 16, 2018

Last Update Submit

May 30, 2018

Conditions

Keywords

quality improvementlong term carepolypharmacy

Outcome Measures

Primary Outcomes (1)

  • Medication regimen

    Active prescriptions

    Four months post intervention

Secondary Outcomes (2)

  • Level of pain

    Four months post intervention

  • Level of agitation

    Four months post intervention

Study Arms (2)

Pre-intervention

NO INTERVENTION

Usual care

Post-intervention

EXPERIMENTAL

One 90-minute interdisciplinary knowledge exchange including the provision of a validated list of appropriate and inappropriate medications for severe dementia long-term care residents.

Behavioral: Knowledge exchange

Interventions

OptimaMed

Post-intervention

Eligibility Criteria

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

You may qualify if:

  • diagnosis of dementia of any etiology
  • severe dementia

You may not qualify if:

  • admission less than 2 months before intervention

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre intégré universitaire de santé et de services sociaux de la Capitale-Nationale

Québec, Canada

Location

Related Publications (1)

  • Kroger E, Wilchesky M, Marcotte M, Voyer P, Morin M, Champoux N, Monette J, Aubin M, Durand PJ, Verreault R, Arcand M. Medication Use Among Nursing Home Residents With Severe Dementia: Identifying Categories of Appropriateness and Elements of a Successful Intervention. J Am Med Dir Assoc. 2015 Jul 1;16(7):629.e1-17. doi: 10.1016/j.jamda.2015.04.002. Epub 2015 May 13.

    PMID: 25979776BACKGROUND

MeSH Terms

Conditions

Dementia

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesNeurocognitive DisordersMental Disorders

Study Officials

  • Edeltraut Kröger, Ph.D.

    Centre intégré universitaire de santé et de services sociaux de la Capitale-Nationale

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
It was unlikely that participants could foresee whether or when their medications have been reviewed or modified.
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SEQUENTIAL
Model Details: Pre-post study
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Adjunct professor

Study Record Dates

First Submitted

May 16, 2018

First Posted

May 29, 2018

Study Start

March 1, 2014

Primary Completion

October 1, 2014

Study Completion

December 1, 2015

Last Updated

June 1, 2018

Record last verified: 2018-05

Data Sharing

IPD Sharing
Will not share

Locations