ClinicalTrials.Veeva

Menu

Web basEd soCial Media tecHnology to Improvement in Adherence to Dual anTiplatelet Therapy Following Drug-Eluting Stent Implantation (WeChat)

G

Guangdong Provincial People's Hospital (Guangdong Provincial Academy of Medical Sciences)

Status

Unknown

Conditions

Coronary Disease

Treatments

Behavioral: Usual Text Messages
Behavioral: Personalized Reminders
Behavioral: Interactive Responses

Study type

Interventional

Funder types

Other

Identifiers

NCT03732066
GDREC2018327H

Details and patient eligibility

About

Few studies have attempt to improve DAPT adherence through social media. The investigators will explore the prevalence of DAPT discontinuation and prove the hypothesis that using social media will improve DAPT adherence among patients requiring DAPT following DES implantation.

Full description

Dual antiplatelet therapy (DAPT) is frequently discontinued after drug-eluting stent (DES) implantation, which could lead to many major adverse cardiovascular events (MACEs). Social media have been proven effective in improving lifestyles and blood pressures control, but few studies have attempt to improve DAPT adherence through social media.Therefore, eligible patients will be enrolled through scanning QR code and randomized in a 1:1 ratio to an intervention group or control group with 12 months of follow-up.The investigators will find out the prevalence of DAPT discontinuation and prove the hypothesis that using social media will improve DAPT adherence among patients requiring DAPT following DES implantation..

Enrollment

760 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged ≥18 years
  • diagnosed CHD and underwent DES implantation
  • provide written informed consent

Exclusion criteria

  • pregnancy
  • malignant tumor or end-stage disease with a life expectancy of <1 year;
  • refusal to use social media
  • refusal to provide written informed consent for this study

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

760 participants in 2 patient groups

Intervention Group
Experimental group
Description:
The intervention group will receive usual text messages, personalized reminders and interactive responses.
Treatment:
Behavioral: Personalized Reminders
Behavioral: Usual Text Messages
Behavioral: Interactive Responses
Control Group
Other group
Description:
The control group will receive usual text messages only.
Treatment:
Behavioral: Usual Text Messages

Trial contacts and locations

1

Loading...

Central trial contact

Yong Liu, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems