Skip to content

Effect of a home-based exercise program on exercise capacity in patients undergoing bypass surgery.

Effectiveness of a home-based prehabilitation program on functional capacity in patients undergoing coronary artery bypass graft surgery - a randomized clinical trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061461
Enrollment
252
Registered
2024-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: Exercise program - Prehabilitation.: The intervention group will receive a home based exercise program that will extend for 2 to 4 weeks before surgery. The patients will be enrolled i

Sponsors

Shrikant Sahu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age more than 18 years. 2. Undergoing elective coronary artery bypass graft surgery. 3. Has at least two weeks of wait period before surgery. 4. Eligible for prehabilitation as per the treating cardiologist and cardiac surgeon.

Exclusion criteria

Exclusion criteria: 1. History of previous cardiac surgery. 2. Severe musculoskeletal or neurological impairments impeding assessment or therapy. 3. Known psychiatric illnesses affecting participation in the program. 4. Class 4 angina on the Canadian Cardiac Society scale. 5. Unstable arrhythmias (Atrial fibrillation with fast ventricular rate, ventricular tachycardia with pulse, high degree AV block, uncontrolled sinus tachycardia). 6. Decompensated heart failure. 7. Severe aortic or mitral stenosis. 8. Acute pericarditis or myocarditis. 9. Patients having ICD or permanent pacemaker. 10. Acute systemic illness or fever. 11. Currently participating in another interventional clinical trial.

Design outcomes

Primary

MeasureTime frame
Six-minute walk distanceTimepoint: T0, At enrolment (Baseline) T1, One day before surgery T2, On the day of discharge after surgery T4, Three months after surgery

Secondary

MeasureTime frame
Barthel IndexTimepoint: T0, At enrolment (Baseline) T1, One day before surgery T3, One month after surgery T4, Three months after surgery;Cardiac self efficacy scaleTimepoint: T0, At enrolment (Baseline) T1, One day before surgery T3, One month after surgery T4, Three months after surgery;Euro QoL 5D-5LTimepoint: T0, At enrolment (Baseline) T4, Three months after surgery;Length of hospital stayTimepoint: T3, On the day of discharge after surgery;Major Adverse Cardiac EventsTimepoint: T1, One day before surgery T2, On the day of discharge after surgery T3, One month after surgery T4, Three months after surgery;Postoperative pulmonary complicationsTimepoint: During hospital stay after surgery until discharge;Tampa scale of kinesiophobia - HeartTimepoint: T0, At enrolment (Baseline) T1, One day before surgery T2, On the day of discharge after surgery T3, One month after surgery T4, Three months after surgery

Countries

India

Contacts

Public ContactShrikant Sahu

Manipal College of Health Professions

shrikant.sahu.pt@gmail.com8108007386

Outcome results

None listed

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