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Impact of Patient Education on Benzodiazepine Use in the Elderly

Impact of Patient Education on Benzodiazepine Use in the Elderly

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02478593
Enrollment
0
Registered
2015-06-23
Start date
2015-06-30
Completion date
2019-01-31
Last updated
2021-10-06

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

Conditions

Anxiety, Insomnia

Keywords

Education, Geriatric, Benzodiazepine, Prevalence

Brief summary

The overall goal of this research is to develop and test strategies to decrease potentially inappropriate medication use among the elderly.

Detailed description

Specifically, the purpose of the study is to determine whether direct patient education is effective in decreasing benzodiazepine use in seniors.

Interventions

Participants in the intervention group will receive an 8-page booklet that includes a list of generic and brand benzodiazepine names, benzodiazepine medication knowledge test, information about the associated risks of benzodiazepine use, and a list of safe alternative to their potentially inappropriate medication, as well as a stepwise tapering method. Recommendations to discuss decreasing use of benzodiazepines with physicians as well as to consult physicians before stopping any medication are also advised in the booklet. Participants in the control group will receive a booklet, produced by the Centers for Disease Control and Prevention, containing information regarding the important of exercise for seniors.

Sponsors

University of Vermont
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Men and women * Full benefit members living in a SASH facility * 60 years old or older * Using at least 1 active short/medium/long acting benzodiazepine at time of recruitment

Exclusion criteria

* Inability to provide consent * Inability to communicate in English * Diagnosis of severe mental illness, dementia, seizure disorder

Design outcomes

Primary

MeasureTime frameDescription
Benzodiazepine or non-benzodiazepine hypnotic medication useBaseline and 6 months post-interventionProportion of subjects using benzodiazepine or non-benzodiazepine hypnotic medication (such as zolpidem)

Secondary

MeasureTime frameDescription
Patient attempt to discontinuing benzodiazepine1 month and 6 months post-interventionNovel patient reported measure regarding attempts to discontinue medication
Patient knowledge regarding benzodiazepinesBaseline and 6 months post-interventionNovel patient reported measure regarding knowledge of the potential risks and benefits of benzodiazepines
Belief about Medicines Questionnaire (BMQ)Baseline and 6 months post-interventionThis is a validated instrument assessing patient beliefs regarding medication efficacy and safety

Outcome results

None listed

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