Pharmacists step in to boost blood thinner adherence in atrial fibrillation patients
NCT ID NCT07159399
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether one-on-one education from a trained pharmacist can help people with atrial fibrillation take their blood thinners (DOACs) as prescribed. About 400 patients will either receive this extra support or usual care. The goal is to see if the education improves medication adherence and reduces stroke risk.
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 education program
- What this could lead to
- If successful, this could show that simple pharmacist education helps patients take their blood thinners more consistently, reducing stroke risk.
- What could go wrong
- This is a behavioral study, not a drug trial. Results depend on patient engagement and may not apply to all populations. The benefit may be modest.
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 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Dec 2031
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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18 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: * 18 years of age or older * have a confirmed diagnosis of AF * are expected to begin DOAC therapy for at least 3 months for stroke prevention Exclusion Criteria: * cannot understand DOAC-related education due to low literacy, language barriers, or cognitive impairment * have been on DOAC therapy for more than 6 months * using DOACs in off-label regimens * are pregnant or breastfeeding
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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National Taiwan University Hospital
Taipei, Taiwan
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