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Clinical Trials in Taiwan / NCT07159399
Enrolling by invitation Not applicable

A Pharmacist-Led Education Program to Improve Adherence to Direct Oral Anticoagulants in Patients With Atrial Fibrillation

NCT07159399 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-03-05
Last updated
2025-09-08

Condition(s) studied

Atrial Fibrillation (AF)

Investigational drug(s) / intervention(s)

Pharmacist-led patient educationUsual Care

Pharmacist-led patient education: Trained pharnacists will provide information on: (1) the indication and the reason of DOAC prescription, (2) the name and the appearance of the DOAC agent, (3) the dose, frequency, time of administration, (4) the mechanism of action, (5) management of missed doses, (6) potential side effects and self-monitoring, and (7) perioperative management. An education leaflet about DOACs will also be provided to improve patients' understanding about the use of DOACs.

Usual Care: Patients in the usual care group will receive only usual care, without pharmacists providing additional DOAC education materials.

Study summary

Atrial fibrillation (irregular heartbeat) increases the risk of stroke, and patients are commonly treated with direct oral anticoagulants (DOACs). However, when patients do not take these medications regularly, the drugs may not work effectively, increasing health risks.

In this study, called PharmAD-AF, specially trained pharmacists will meet with patients who have atrial fibrillation and are prescribed DOACs. They will offer personalized education and support to help patients take their medications as directed.

Researchers will compare groups of patients who receive this pharmacist-led education versus those who receive usual care. The main goals are to assess whether pharmacist support improves how consistently patients take their DOACs and how well the treatment prevents strokes while avoiding the side effects of DOAC therapy.

If successful, the study will demonstrate how pharmacist-led education can help patients stick to their treatment plan and reduce serious health risks, offering a practical way to improve heart-related care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Taiwan University Hospital Taipei Taiwan

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07159399 on ClinicalTrials.gov ↗ ← All trials in Taiwan