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The Impact of Audiovisual Structured Patient Education Material in Improving Clinical and Behavioural Outcomes in Home-Based Cardiac Rehabilitation Programme Participants

NCT07636460 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2026-06-09

No results posted yet for this study

Summary

The goal of this clinical trial is to find out if newly developed, culturally adapted educational videos-sent through a mobile messaging app-can help people with coronary heart disease do better in a home-based cardiac rehabilitation program in Malaysia.

The main questions it aims to answer are:

* Do the educational videos help participants improve their fitness?
* Do the videos help participants better understand heart health and stick to a healthy lifestyle?

Researchers will compare the educational videos to existing standard educational materials to see if the video-based education is more helpful for supporting rehabilitation at home.

Participants will:

* Take part in a 12-week home-based cardiac rehabilitation program
* Receive either educational videos or standard education materials
* Meet with the cardiac rehabilitation team every 4 weeks
* Complete a treadmill exercise test, blood tests, and questionnaires before and after the program.

Conditions

  • Coronary Arterial Disease (CAD)
  • Myocardial Infarction (MI)
  • Ischemic Heart Disease (IHD)
  • Cardiac Rehabilitation
  • Educational Intervention

Interventions

OTHER

Audiovisual Structured Patient Education Materials

Bilingual (Malaysian and English language) Audiovisual Structured Patient Education Materials that are culturally adaptable on secondary prevention cardiac risk factors, self-care and exercise recommendations.

OTHER

Standard Educational Materials

Standard visual-based educational materials currently used in Cardiac Rehabilitation Programme Phase 2, Universiti Malaya Medical Centre

Sponsors & Collaborators

  • University of Malaya

    lead OTHER

Principal Investigators

  • Anwar Suhaimi · University of Malaya

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-19
Primary Completion
2025-01-08
Completion
2025-01-16

Countries

  • Malaysia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07636460 on ClinicalTrials.gov