Skip to content

APP-based Multifaceted Management After PCI

Mobile Application-based Multifaceted Management to Improve Long-term Care After Percutaneous Coronary Intervention

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03059784
Enrollment
1100
Registered
2017-02-23
Start date
2017-03-31
Completion date
2018-08-31
Last updated
2017-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Percutaneous Coronary Intervention

Brief summary

High rates of recurrent cardiovascular events and readmission after percutaneous coronary intervention (PCI) are important issues. Guidelines emphasize rehabilitation and secondary prevention. But many patients are lack of effective management after PCI.This study is aimed to examine the effect of mobile application (APP)-based multifaceted management on the improvement of long-term care after PCI.

Detailed description

This is a cluster-randomized controlled trial to evaluate the effect of APP-based multifaceted management strategy on improvement of long-term care for medication adherence,risk factor control, and reduction of adverse events, readmission rate and mortality after PCI.It includes knowledge education, medication reminder,advice provision, support to change lifestyle behaviors. The program is interactive between care provider and patients. A total of 20 wards will be randomly assigned to intervention or usual care.Anticipated 1100 patients after PCI will be participated in the trial. All the participants will be followed up until 12 months.

Interventions

OTHERAPP-based multifaceted management

Patients after PCI will be regularly given education materials, medication reminders, life-style behaviors instruction through APP. Cardiologists can interact with patients on advice provision and clinical support after discharge through APP.

Sponsors

Chinese Academy of Medical Sciences, Fuwai Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients who have received percutaneous coronary intervention and are discharged alive in the study centers; * patients who are able to use APP; * patients who provide informed consent.

Exclusion criteria

* patients who are not able to use APP; * dementia; * mental disturbed; * patients who are not willing to receive management and follow up.

Design outcomes

Primary

MeasureTime frameDescription
evidence-based medication adherence (the proportion of participants taking 3 medications (aspirin, P2Y12 receptor inhibitor, statin) without contraindications)at 12 months after PCIthe proportion of participants taking 3 medications (aspirin, P2Y12 receptor inhibitor, statin) without contraindications

Secondary

MeasureTime frameDescription
rate of LDL-C achieving targetat 12 months after PCIrate of LDL-C achieving target based on guideline
rate of systolic blood pressure achieving targetat 12 months after PCIrate of systolic blood pressure achieving target based on guideline
readmission rate12 months after PCIreadmission rate after PCI

Other

MeasureTime frameDescription
smoking status (the proportion of participants with smoking cessation)at 12 months after PCIthe proportion of participants with smoking cessation
rehabilitation (the proportion of participants who receive rehabilitation program)12 months after PCIthe proportion of participants who receive rehabilitation program

Contacts

Primary ContactHAIYAN XU
hyxu@yahoo.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026