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Effectiveness of Phase I Cardiac Rehabilitation among Patients Undergoing CABG Surgery - A Randomized Controlled Trial

Effectiveness of phase I cardiac Rehabilitation on postoperative outcome among patients undergoing coronary artery Bypass grafting surgery in a tertiary care center Thiruvananthapuram, RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/031176
Enrollment
70
Registered
2021-02-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: I00-I99- Diseases of the circulatory system

Interventions

Intervention1: Phase I Cardiac Rehabilitation: Formal permission for data collection will be obtained from institutional research committee, ethics committee, Medical College Hospital, Thiruvananthapu

Sponsors

Remya JM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients admitted for routine coronary artery bypass grafting surgery for the first time at a tertiary care centre. 2. Patients who are willing to participate in the study. 3. Patients who are able to read and write Malayalam.

Exclusion criteria

Exclusion criteria: 1. Patients having severe LV dysfunction. 2. Coronary artery bypass grafting surgery on emergency basis. 3. Patients having psychological disturbances who cannot able to follow instructions.

Design outcomes

Primary

MeasureTime frame
the investigator assume that there is change in cardiac function respiratory function wound infection, and anxiety level of CABG patients experimental group than in control group Timepoint: The primary outcome is assessed within 45 days. The assessment will be done preoperatively, postoperatively (3rd day), before discharge and first follow-up

Secondary

MeasureTime frame
the investigator assumes that there is difference in cardiac function, respiratory function, wound infection, and anxiety level of CABG patients in experimental group than in control groupTimepoint: within 45 days

Countries

India

Contacts

Public ContactRemya J M

College of Nursing, Thiruvananthapuram

preethynair79@rediffmail.com8139005157

Outcome results

None listed

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