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NCT07683143Completed

A Nurse-Led Program to Improve Patient Health Promotion Behaviors Among Elderly Patients After PCI

Construction And Application Of An IMB Model-Based Health-Promoting Behavior Intervention Program For Elderly Patients With Coronary Heart Disease After PCI

Source: ClinicalTrials.gov · Last updated 6 Jul 2026

Brief summary (registry, in English)

The goal of this study is to develop and evaluate a nurse-led intervention program based on the Information-Motivation-Behavioral Skills (IMB) model to improve health-promoting behaviors and quality of life in elderly patients after percutaneous coronary intervention (PCI). It will also learn about the program's effects on self-efficacy and relevant objective clinical indicators. The main questions it aims to answer are: Does the IMB-based nurse-led intervention improve health-promoting behaviors in elderly PCI patients? What effects does the intervention have on patients' self-efficacy, quality of life, and objective clinical indicators? Researchers will compare the nurse-led IMB-based intervention to usual care to see if the program effectively enhances health-promoting behaviors and quality of life. Participants will: Receive the IMB-based nurse-led intervention or usual care Be followed up for a specified period with regular assessments Complete questionnaires on health-promoting behaviors, self-efficacy, and quality of life at baseline and at designated time points post-intervention Have objective clinical indicators measured and recorded

Status (registry)
Completed
Study type
Interventional
Enrollment
78 (actual)
First submitted
24 Jun 2026
Start date
2 May 2025
Primary completion date
20 Nov 2025
Lead sponsor
Henan University
NCT number
NCT07683143

What you commit to

  • Study type: Interventional
  • Participants enrolled: 78
  • From 2 May 2025 to the primary completion date, 20 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • severe concomitant diseases affecting vital organs (e.g., liver, brain, or kidneys)

Other

  • current participation in other similar studies

Who the study is looking for

  • a confirmed diagnosis of coronary heart disease with a stable condition following PCI
  • age ≥60 years
  • normal cognitive and communication abilities
  • provision of written informed consent and voluntary participation in the study

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Huaihe Hospital of Henan University
Coordinator of this site? Confirm its status
KaifengChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.