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Clinical Trials/NCT06034444
NCT06034444CompletedNot Applicable

Better tArgetting, Better Outcomes for Frail ELderly Patients: A Quality Improvement Initiative in Long-term Care Facilities Using interRAI Long-term Care Assessment in Quebec

Centre hospitalier de l'Université de Montréal (CHUM)1 site in 1 country5,692 target enrollmentStarted: August 16, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
5,692
Locations
1
Primary Endpoint
Change in falls prevalence

Study Overview

Brief Summary

The acronym for this proposal, BABEL, refers to the fact that a common "language" - the interRAI risk-stratification and decision-making tool - will be used in this project, allowing several measures of care quality in long-term care facilities to be compared with those in other provinces for the first time. The impact of the use of this assessment system and associated care planning protocols will also be investigated using usual practice as the point of reference.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All nursing home residents in a particular unit where standardized evaluations are being introduced (for example, all residents in a particular floor or wing of the longterm care facility)

Exclusion Criteria

  • Residents who are admitted to a nursing home unit for less than 1 week.

Outcomes

Primary Outcomes

Change in falls prevalence

Time Frame: Every 3 months, for a minimum of 6 months and a maximum of 36 months

Prevalence of falls among residents under study

Change in prevalence of pain

Time Frame: Every 3 months, for a minimum of 6 months and a maximum of 36 months

Using interRAI pain scale scores greater than 0

Change in depression prevalence

Time Frame: Every 3 months, for a minimum of 6 months and a maximum of 36 months

Depression rating scale score of 3 or more (from interRAI LTCF)

Change in prevalence of potentially inappropriate antipsychotic use

Time Frame: Every 3 months, for a minimum of 6 months and a maximum of 36 months

Use of antipsychotics in the absence of an appropriate diagnosis

Change in the prevalence of physical restraints use

Time Frame: Every 3 months, for a minimum of 6 months and a maximum of 36 months

Use of physical restraints on residents as assessed using interRAI LTCF

Secondary Outcomes

  • Change in prevalence of pressure ulcers(Every 3 months, for a minimum of 6 months and a maximum of 36 months)

Investigators

Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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