Can a Pharmacist's call after discharge slash readmissions?
NCT ID NCT04071951
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether having a pharmacist review medications and counsel patients before and after hospital discharge can reduce return trips to the hospital or ER within 30 days. Over 6,400 older adults (55+) taking many medications or high-risk drugs are taking part. The pharmacist helps with medication lists, adherence, and simplifying complex drug regimens.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pharmacist-led medication management and counseling
- What this could lead to
- If it works, this could reduce hospital readmissions and emergency visits for older adults taking many medications.
- What could go wrong
- This is a behavioral intervention, not a drug, so results may vary by hospital and patient adherence. The study is pragmatic, meaning real-world factors could dilute the effect.
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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6,478 people
The number who actually took part.
- Started
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Dec 2019
- Expected to finish
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Jan 2027
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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55 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Admitted to a medical ward, AND * \> 55 years AND * ≥ 10 prescription medications at admission OR • ≥ 3 high-risk medications (anticoagulants, antiplatelets, insulin, oral hypoglycemics) at admission Exclusion Criteria: * Expected discharge to another state, acute care facility, psychiatric facility, or locked facility (including locked skilled nursing facility, jail, or prison) OR * Expected AMA or left hospital against medical advice (AMA) OR * Homeless OR * On hospice OR * Already enrolled into study within the past year OR * Patients admitted by admitting or attending Primary Medical Doctors who have a specialty that is not Internal Medicine or Family Medicine OR * Expected to receive pharmacist-led peri- and post-discharge medication management regardless of the trial OR * Expected post-discharge setting not conducive to the studied medication management intervention (e.g. SNF, rehabilitation facility) OR * Patients admitted with a suspected or confirmed diagnosis of COVID-19.
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Conditions
The condition(s) this trial relates to.
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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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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Cedars-Sinai Medical Center
Los Angeles, California, 90048, United States
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Other studies related to the condition(s) this trial covers.
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