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

NCT06317376 | Completed

• 1 other identifier: REC/014131 Maria Haseen
• Study Type: interventional
• Target: 54
• Locations: 1 country
• Sites: 1

Brief Summary

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

Conditions

Post-cardiac Surgery

Outcome Measures

Primary Outcomes (2)

• 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

• 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

Study Arms (2)

experimental group (MICT)

EXPERIMENTAL

MICT 3 session per week with Aerobic exercise on treadmill for 30 minute with moderate intensity.

Other: MICT with Aerobic exercise on treadmill

control group (standard protocol)

OTHER

Perform standard hospital protocol 2-3 session per week

Other: standard hospital protocol

Interventions

MICT with Aerobic exercise on treadmill OTHER

MICT 3 session per week with Aerobic exercise on treadmill for 30 minute with moderate intensity.

experimental group (MICT)

standard hospital protocol OTHER

standard hospital protocol

control group (standard protocol)

Eligibility Criteria

• Age: 40 Years - 60 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Males and females post CABG patients with ages of 40 to 60 years postoperatively.
• The patient with Post Op-Day 5.

You may not qualify if:

• 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

Sponsors & Collaborators

• Riphah International University: lead

Study Sites (1)

RMI

Peshawar, Pakistan

Location

Study Officials

• Maria Razzaq, MS

  Riphah International University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 18, 2024
• First Posted: March 19, 2024
• Study Start: September 1, 2023
• Primary Completion: January 15, 2024
• Study Completion: January 18, 2024
• Last Updated: March 19, 2024

Record last verified: 2024-03

Data Sharing

• IPD Sharing: Will not share

Locations

PA (1)