ClinicalTrials.Veeva

Menu

Effect of eHealth Cardiac Rehabilitation Incorporating Mindfulness for Patients With Coronary Heart Disease (eCR)

T

Tung Wah College

Status

Enrolling

Conditions

Coronary Heart Disease (CHD)

Treatments

Behavioral: eHealth cardiac rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT07109752
REC2024214 (Other Identifier)
TungWC REC2024214

Details and patient eligibility

About

People with coronary heart disease (CHD) often feel more stressed, which can increase the risk of having another heart problem. Cardiac rehabilitation (CR) is a common treatment for those with CHD, focusing on changing lifestyles and managing the disease. However, it often does not address stress management adequately. There is also a lack of psychological therapy and involvement of mental health professionals in online CR programs. Because traditional CR programs have low participation rates, online platforms are becoming more popular for providing rehabilitation support. This is important because more than half of people with CHD report high stress levels, which can cause or worsen heart problems. To address this issue, the proposed study will test an online CR program that includes mindfulness to help manage stress for CHD patients.

Full description

The proposed project is a study designed to test the effects of an online cardiac rehabilitation program, which includes mindfulness, on stress and health outcomes for people with coronary heart disease (CHD). The study will last 12 weeks and will be structured as a single-blinded, two-group randomized controlled trial. This means that participants will be randomly assigned to either the treatment group or a control group, and they won't know which group they're in. After the trial, there will be an evaluation to gather more in-depth insights.

Participants will be asked to complete assessments using questionnaires and activity monitors at the start of the study, at 6 weeks, and at 12 weeks. Each assessment will take about 40 minutes, and there will also be a 30 to 40-minute interview.

Those in the intervention group will have a face-to-face meeting to set goals and learn how to use the CR website and activity monitors, which will take about 50 minutes. They will be encouraged to use the website weekly to learn about healthy lifestyle changes, like walking briskly for 30 minutes a day, eating a healthy diet, listening to mindfulness audios, and not smoking. A nurse will call them every two weeks for the first six weeks to check in.

The study is led by an Assistant Professor who has the necessary office space and access to various facilities to support the research. She specializes in cardiovascular health and has established connections in the field of cardiac rehabilitation, which are valuable for successfully conducting the study.

The team includes co-investigators with expertise in physiotherapy, exercise rehabilitation, psychiatric nursing, and intensive care nursing, ensuring the study is well-supported and that results are properly reported and published.

Enrollment

146 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

People will be eligible for this study if they were:

  1. diagnosed with CHD (within the past 6 months),
  2. undergone conservative treatment, such as percutaneous coronary intervention (PCI) and/ or medication,
  3. currently under stable medication regimen and discharged to home.
  4. aged 18 years or older,
  5. reported scores ranging from 3 (to some degree) to 5 (very much) scores on a single-item stress symptoms scale (Elo et al., 2003),
  6. using a computer and/or smartphone to access the Internet at home,
  7. and, read and speak Chinese.

Exclusion criteria

  1. diagnosis of acute psychotic disease;
  2. presence of a life-limiting condition;
  3. prescribed contradictions to physical activity; and,
  4. presence of hearing, visual, or ambulatory disorders

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

146 participants in 2 patient groups

eCR
Experimental group
Description:
Intervention arm
Treatment:
Behavioral: eHealth cardiac rehabilitation
Control
No Intervention group
Description:
Usual care

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Jingjing Su, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems