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CompletedNCT06034444BABELUpdated Sep 13, 2023

Better tArgetting, Better Outcomes for Frail ELderly Patients

An observational study in Residents in Longterm Care Facilities, sponsored by Centre hospitalier de l'Université de Montréal (CHUM). Completed at 1 site in Canada. Per ClinicalTrials.gov, last updated 2023-09-13.

Sponsored by Centre hospitalier de l'Université de Montréal (CHUM) · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
5,692
Sex
All
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Study 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.

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Conditions studied

  • Residents in Longterm Care Facilities
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In context

Lead sponsor

Centre hospitalier de l'Université de Montréal (CHUM) is the lead sponsor of 370 studies on the registry; 110 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Residents in a long-term care facility (nursing home)

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

Exclusion Criteria:

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

Observational model
Cohort
Time perspective
Prospective
Enrollment
5,692 participants (actual)
Patient registry
No

Groups and cohorts

  • interRAI LTCF

    Nursing homes in Quebec where interRAI evaluations and care plans will be introduced.

    Other: interRAI LTCF

Interventions

  • OtherinterRAI LTCF

    Standardized evaluations (interRAI LTCF) will be introduced to selected nursing homes in Quebec.

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What researchers measure

Primary outcomes

  1. Change in depression prevalence

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

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

  2. Change in prevalence of potentially inappropriate antipsychotic use

    Use of antipsychotics in the absence of an appropriate diagnosis

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

  3. Change in falls prevalence

    Prevalence of falls among residents under study

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

  4. Change in prevalence of pain

    Using interRAI pain scale scores greater than 0

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

  5. Change in the prevalence of physical restraints use

    Use of physical restraints on residents as assessed using interRAI LTCF

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

Secondary outcomes

  1. Change in prevalence of pressure ulcers

    Stage 2 pressure ulcer on the interRAI pressure ulcer scale

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

Other outcomes

  1. Change in other interRAI LTCF quality indicators

    interRAI LTCF evaluation leads to a number of quality indicators being generated each of which will be tracked over time for each facility to compare before and after effects, as well as comparisons with other centers in Canada

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

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Study locations

1 site
  • Donald Berman Maimonides
    Montréal, Quebec H4W 2Y6, Canada
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 13, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06034444
Lead sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Collaborators
Canadian Frailty Network
Responsible party
Sponsor
First posted
Sep 13, 2023
Start date
Aug 16, 2018
Primary completion
Mar 31, 2020
Completion
Mar 31, 2020
Last update
Sep 13, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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