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Clinical Trials in China / NCT07174778
Starting soon Not applicable

Episodic Future Thinking to Improve Anticoagulant Adherence in Atrial Fibrillation

NCT07174778 · tracked via the Priya Life Science China tracker
Sponsor
Jiawen You
Phase
Not applicable
Started
2025-09-15
Last updated
2025-09-16

Condition(s) studied

Atrial Fibrillation (AF)

Investigational drug(s) / intervention(s)

Episodic future thinkingattention control

Episodic future thinking: Participants will engage in episodic future thinking prompted via text-based cues and picture-based cues to help them adhere to oral anticoagulants. Participants will also receive health education on atrial fibrillation-related stroke prevention.

attention control: The control group will receive standard care, including routine health education from ward nurses and one post-discharge telephone follow-up. In additon, participants will receive a message from the researcher at the same time point each day, but the message will only involve daily greetings.

Study summary

The purpose of this study is to assess the effectiveness of Episodic Future Thinking (EFT) on improving medication adherence in atrial fibrillation (AF) patients taking oral anticoagulants. A total of 68 participants will be randomly assigned to the intervention group or the control group. Those in the intervention group will receive a 3-week EFT intervention in addition to the usual care, while those in the control group will receive the usual care only. Data on medication adherence, delay discounting (DD), and anticoagulation knowledge will be collected at baseline, end of intervention, and 3-month follow-up.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Meets diagnostic criteria for atrial fibrillation per the Chinese Guidelines for the Diagnosis and Management of Atrial Fibrillation, with clinically stable condition * Current or previous use of oral anticoagulants * Age ≥18 years * Capable of using WeChat mobile application * Willing to provide informed consent Exclusion Criteria: * Comorbid severe impairment of major organ systems or end-stage disease * Significant visual or auditory impairments * Documented cognitive dysfunction or psychiatric disorders (e.g., major depressive disorder, schizophrenia, bipolar disorder)

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Guangdong Provincial People's Hospital Guangzhou Gangdong
The First Affiliated Hospital of Sun Yat-sen University Guangzhou Gangdong

Other trials for the same condition

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 NCT07174778 on ClinicalTrials.gov ↗ ← All trials in China