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CompletedNCT07346664Updated Jan 16, 2026

Medication Adherence and Lipid Management in Patients With Coronary Heart Disease After Percutaneous Coronary Intervention: Application of the Transitional Care Model

An interventional study of routine nursing care group and TCM intervention group in Transitional Care Model, Coronary Heart Disease and Medication Adherence, sponsored by Qing Wang. Completed at 1 site in China. Open to participants aged 47 Years to 58 Years. Per ClinicalTrials.gov, last updated 2026-01-16.

Sponsored by Qing Wang · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 3 years 5 months after the study started (first participant enrolled Jul 2022, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
108
Allocation
Randomized
Ages
47 Years to 58 Years
Sex
All
01

Study summary

Patients with coronary heart disease (CHD) require long-term medication and lifestyle modification following percutaneous coronary intervention (PCI). However, they often face challenges such as poor medication adherence and inadequate self-management. This study aims to evaluate the effects of the transitional care model (TCM) on CHD patients after PCI, regarding medication adherence, self-efficacy, and lipid levels.

Read the detailed description

TCM improved medication adherence, self-efficacy, and lipid profiles in CHD patients after PCI, while enhancing overall patient satisfaction. Compared with routine nursing care, TCM yielded superior clinical benefits and is recommended for broader application in the post-PCI management of CHD patients.

02

Conditions studied

  • Transitional Care Model
  • Coronary Heart Disease
  • Medication Adherence
  • Self-efficacy
  • Lipid Profile
03

In context

Coronary Disease

2,839 studies on the registry are indexed under Coronary Disease; 311 are open to participants now.

This study's enrollment of 108 is below the median of 124 across 1,583 interventional studies indexed under Coronary Disease.

Browse Coronary Disease studies →

Lead sponsor

This is the only study on the registry with Qing Wang as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
47 Years to 58 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • patients clinically diagnosed with CHD according to established diagnostic criteria
  • patients who met the World Health Organization (WHO) indications for PCI
  • complete clinical data available

Exclusion criteria

Exclusion Criteria:

  • Patients with cognitive impairment
  • Patients with incomplete follow-up data.
  • Patients with comorbid malignancy
  • Patients with severe hepatic
  • Patients with renal insufficiency
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
108 participants (actual)

Study arms

  • Other
    routine nursing care group

    Patients assigned to the control group underwent routine nursing care based on the standardized medical treatment, including admission health education (PCI postoperative risk management and medication instructions), psychological counseling, dietary and exercise guidance, individualized rehabilitation planning, and discharge instructions. After discharge, patients attended routine outpatient follow-up visits, including laboratory testing of blood lipids, blood pressure, and blood glucose, without structured follow-up or WeChat-based education. Routine outpatient education and guidance were provided only.

    Other: routine nursing care group

  • Other
    TCM intervention group

    Patients in the observation group received a 3-month TCM intervention delivered by specially trained nurses, in addition to routine nursing care.

    Other: TCM intervention group

Interventions

  • Otherroutine nursing care group

    Patients assigned to the control group underwent routine nursing care based on the standardized medical treatment, including admission health education (PCI postoperative risk management and medication instructions), psychological counseling, dietary and exercise guidance, individualized rehabilitation planning, and discharge instructions. After discharge, patients attended routine outpatient follow-up visits, including laboratory testing of blood lipids, blood pressure, and blood glucose, without structured follow-up or WeChat-based education. Routine outpatient education and guidance were provided only.

  • OtherTCM intervention group

    Patients in the observation group received a 3-month TCM intervention delivered by specially trained nurses, in addition to routine nursing care.

06

What researchers measure

Primary outcomes

  1. Medication Adherence

    Medication adherence will be assessed using the Medication Adherence Report Scale-5 (MARS-5). The scale consists of 5 items that evaluate nonadherent behaviors (e.g., forgetting to take medications, altering dosages). Each item is scored on a 5-point Likert scale (1="always" to 5="never"), with total scores ranging from 5 to 25. A higher total score indicates better medication adherence.

    Time frame: Baseline (before discharge) and 3 months after discharge

Secondary outcomes

  1. Self-efficacy

    Self-efficacy will be assessed using the General Self-Efficacy Scale (GSS). The GSS is a validated 16-item instrument, with each item scored from 0 to 4. Higher total scores reflect greater self-efficacy in managing health and adhering to treatment recommendations.

    Time frame: Baseline (before discharge) and 3 months after discharge

  2. Lipid Profile

    Fasting serum levels of total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) will be measured using an automated biochemical analyzer. All measurements will be performed in mmol/L.

    Time frame: Baseline (before discharge) and 3 months after discharge.

07

Study locations

1 site
  • Northern Jiangsu People's Hospital Affiliated to Yangzhou University
    Yangzhou, Jiangsu 225001, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07346664
Lead sponsor
Qing Wang
Responsible party
Qing Wang (Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Northern Jiangsu People's Hospital) — Sponsor-investigator
First posted
Jan 16, 2026
Start date
Jul 11, 2022
Primary completion
May 9, 2024
Completion
May 26, 2024
Last update
Jan 16, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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