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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061301
Enrollment
40
Registered
2024-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I219- Acute myocardial infarction, unspecified

Interventions

Intervention1: Exercise Training: 3 Months of e-Media supported Exercise Training that includes : 1st Month-Aerobic training
2nd Month-Aerobic and Resistance training
3rd Month-Aerobic, Resistance and Flexibility training
Frequency- 5 days per week
Total Duration - 12 weeks Control Intervention1: Usual Care: Control Group will be given usual care including Counselling and Education on Lifestyle Modification. The Pre Test data will be collected

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
1.Functional Capacity-6 minute walk Test 2.Rating of Perceived Exertion-BORG scaleTimepoint: 12 Weeks

Secondary

MeasureTime frame
1.Quality of Life- WHOQOL-BREF 2.Physical Activity-GPAQTimepoint: 12 Weeks

Countries

India

Contacts

Public ContactManoj Kumar R

Sri Ramachandra Institute of Higher Education and Research

senthilkumar.t@sriramachandra.edu.in8248172742

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026