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Better tArgetting, Better Outcomes for Frail ELderly Patients

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06034444
Acronym
BABEL
Enrollment
5692
Registered
2023-09-13
Start date
2018-08-16
Completion date
2020-03-31
Last updated
2023-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Residents in Longterm Care Facilities

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.

Interventions

OTHERinterRAI LTCF

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

Sponsors

Canadian Frailty Network
CollaboratorOTHER
Centre hospitalier de l'Université de Montréal (CHUM)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
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.

Design outcomes

Primary

MeasureTime frameDescription
Change in the prevalence of physical restraints useEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsUse of physical restraints on residents as assessed using interRAI LTCF
Change in prevalence of potentially inappropriate antipsychotic useEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsUse of antipsychotics in the absence of an appropriate diagnosis
Change in falls prevalenceEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsPrevalence of falls among residents under study
Change in prevalence of painEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsUsing interRAI pain scale scores greater than 0
Change in depression prevalenceEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsDepression rating scale score of 3 or more (from interRAI LTCF)

Secondary

MeasureTime frameDescription
Change in prevalence of pressure ulcersEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsStage 2 pressure ulcer on the interRAI pressure ulcer scale

Other

MeasureTime frameDescription
Change in other interRAI LTCF quality indicatorsEvery 3 months, for a minimum of 6 months and a maximum of 36 monthsinterRAI 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

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026