Nursing home drug safety study aims to cut risky prescribing
NCT ID NCT07407387
First seen Jun 27, 2026 · Last updated Aug 26, 2026 · Updated 2 times
Summary
This study tests whether a team of clinical pharmacologists can help reduce unsafe medication use in nursing homes. Researchers will review each resident's medications, give feedback to staff, and provide education. The study involves 219 residents aged 65+ in seven Swiss nursing homes, comparing outcomes before and after the intervention.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could show that a structured medication review by clinical pharmacologists reduces unsafe prescribing and improves health outcomes for elderly nursing home residents.
- What could go wrong
- This is a small, non-randomized study with no control group, so results may not be generalizable. The intervention is complex and may be difficult to implement in other settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 219 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Expected to remain in the nursing home for the duration of the study * Able to provide informed consent or having a legally authorized representative able to provide consent if the resident lacks capacity Exclusion Criteria: * Residents in their probable last hours or days of life * Residents with moderate to severe cognitive impairment (Cognitive Performance Scale, CPS, score \>4 * Residents housed in assisted nursing home wards, including those requiring palliative care (either in dedicated palliative units or receiving palliative care in general wards), those in the hemodialysis unit, and those with severe obesity (body mass index \>=40kg/m2)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Institute of Pharmacological Science of Southern Switzerland, Ente Ospedaliero Cantonale
Lugano, 6900, Switzerland
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