Effects of e-Media Supported Exercise Based Phase II Cardiac Rehabilitation in Heart Bypass Surgery Patients- A Randomized Controlled Trial

Phase 3

Completed

• Conditions: Health Condition 1: I219- Acute myocardial infarction, unspecified

• Registration Number: CTRI/2024/01/061301
• Lead Sponsor: il

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 24 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

1. Adult patients (age: 35 to 65 years) who have undergone Coronary Artery Bypass

Grafting (CABG) surgery

2. Patients in the Phase II cardiac rehabilitation stage, indicating that they have completed

10

the initial recovery period after surgery and are ready to engage in exercise-based

rehabilitation.

3. Patients who are deemed suitable for home-based cardiac rehabilitation- Low cardiac

risk stratification

4. Patients with access to electronic media devices (e.g., computer, smartphone, tablet)

and internet connectivity.

5. Patients who can understand and communicate effectively in the language used for the

study materials and assessments.

Exclusion Criteria

1. Patients with severe cognitive impairments or mental health conditions that may hinder

their ability to engage in the cardiac rehabilitation program or provide informed consent.

2. Patients with significant comorbidities or medical conditions that would limit their

ability to safely participate in a home-based cardiac rehabilitation program

3. Patients with contraindications to exercise or significant medical conditions that may

affect their ability to safely participate in the rehabilitation program.

4. Patients who have participated in a structured cardiac rehabilitation program within the

past six months.

5. Patients who are unable or unwilling to comply with the study requirements or follow

the assigned e-media supported rehabilitation program.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Functional Capacity-6 minute walk Test <br/ ><br>2.Rating of Perceived Exertion-BORG scaleTimepoint: 12 Weeks

Secondary Outcome Measures

Name	Time	Method
1.Quality of Life- WHOQOL-BREF <br/ ><br>2.Physical Activity-GPAQTimepoint: 12 Weeks