Group-based Cardiac Rehabilitation on Patients With Coronary Artery Bypass Graft Surgery

Post-cardiac Surgery Clinical Trial

Official title:

The Effect of Group-based Cardiac Rehabilitation on Pulmonary Function and Aerobic Capacity of Patients With Coronary Artery Bypass Graft Surgery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06317376
• Other study ID #: REC/014131 Maria Haseen
• Status: Completed
• Phase: N/A
• Start date: September 1, 2023
• Est. completion date: January 18, 2024

Study information

• Verified date: March 2024
• Source: Riphah International University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

1. To determine the effect of Moderate intensity continuous training on Pulmonary function of CABG patients.

2. To determine the effect of MICT on aerobic Capacity of CABG patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 54
• Est. completion date: January 18, 2024
• Est. primary completion date: January 15, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 60 Years

Eligibility

Inclusion Criteria:

• Males and females post CABG patients with ages of 40 to 60 years postoperatively.

• The patient with Post Op-Day 5.

Exclusion Criteria:

• Patients who have a history of other Cardiac disorders that interfere with daily life before surgery and those having congenital cardiac anomalies, Tetralogy of Fallot.

• Musculoskeletal and neurological disorders.

• Age more than 60 and less than 40

Related Conditions & MeSH terms

• Post-cardiac Surgery

Intervention

Other:
• MICT with Aerobic exercise on treadmill
MICT 3 session per week with Aerobic exercise on treadmill for 30 minute with moderate intensity.
• standard hospital protocol
standard hospital protocol

Locations

Country	Name	City	State
Pakistan	RMI	Peshawar

Sponsors (1)

Lead Sponsor	Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Borg rating of perceived exertion scale	This scale is used to measure the appearance of the body in the reacttowith the exertion according to the vital sign and symptoms like increased heart rate, respiratory rate, sweating and muscle tiredness. This scale is ranged from 6 to 20 ranking, in thesrankingsng 6 represents "no exertion at all" and twenty reported "maximal exertion during activity". If participants reporta as 12 to 14 score othe n Borg scale this indicate that exertion is at moderate level during exertion. This scale will be used to measure the level of fatigue over all activity of life	4 weeks
Primary	6min walk test	6 min walk test is used to measure the functional status of the individuals. It will be done on both groups to measure the functional status.	4weeks