Skip to content

An Intervention Study to Reduce the Use and Impact of Potentially Inappropriate Medications Among Older Adults

The Patient as a Driver of Change: an Intervention Study to Reduce the Use and Impact of Potentially Inappropriate Medications Among Older Adults

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01148186
Enrollment
300
Registered
2010-06-22
Start date
2010-06-30
Completion date
2013-05-31
Last updated
2013-05-15

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

Conditions

Anxiety, Incontinence, Insomnia, Polypharmacy

Keywords

Polypharmacy, Benzodiazepine use, Oxybutynin use, cognition disorders/drug therapy, incontinence

Brief summary

An educational intervention targeting community-dwelling older adults will lead to a reduction in potentially inappropriate prescriptions (e.g. benzodiazepines, oxybutynin). Cessation of potentially inappropriate medications (e.g. benzodiazepines, oxybutynin)will lead to improved cognitive outcomes in older adults.

Detailed description

This study tests the effectiveness of a knowledge transfer tool for empowering patients to engage in collaborative discontinuation of potentially inappropriate medication with their pharmacist and/or physician

Interventions

BEHAVIORALknowledge transfer tool

knowledge transfer tool for empowering patients to engage in collaborative discontinuation of potentially inappropriate medication with their pharmacist and/or physician

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 65 year old human adults * who fill a prescription for at least 5 medications * community dwelling * chronic use (3 months or longer) of at least one potentially inappropriate medication (e.g. benzodiazepine, oxybutynin)

Exclusion criteria

* patients with severe mental illness, dementia and epilepsy * concomitant consumption of any other antipsychotic medication (including lithium, olanzapine, clozapine, quetiapine, risperidone, haloperidol etc.) * concomitant consumption of any antiepileptic (including carbamazepine, valproate, gabapentin, lamotrigine, topiramate, oxcarbazepine etc.) * concomitant consumption of a cholinesterase inhibitor or memantine

Design outcomes

Primary

MeasureTime frame
Complete discontinuation of the targeted potentially inappropriate medication (e.g. benzodiazepines, oxybutynin)6 months post-intervention

Secondary

MeasureTime frameDescription
Cognitive function6-months post-interventionMontreal cognitive assessment instrument Rey's auditory verbal learning test (immediate memory, learning, and delayed recall)
Sleep efficiency6-monthsSleep efficiency as documented with a sleep diary
incontinence-related self-efficacy6-months post-interventionincontinence-related self-efficacy as measured with the geriatric self-efficacy index
frequency of urinary incontinence episodes6-months post-interventionfrequency of urinary incontinence as measured with a 72-hour bladder diary

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026