Effects of IMT ON Dyspnea, PF and Quality of Life in Patients With CABG

Not Applicable

Completed

• Conditions: Exercise
• Interventions: Other: Inspiratory muscle training; Other: physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs.

• Registration Number: NCT05936879
• Lead Sponsor: Riphah International University

Brief Summary

Patient in the Intervention group will be treated with routine pysical therapy, Inspiratory muscle training and early ambulation after surgery, whereas patients in the control group will be not be treated with these interventions and will rather undergo routine physical therapy (ankle pumps, hand pumps isometrics of upper and lower limbs).

Patients in the intervention group will receive treatment until discharge from hospital.

Detailed Description

A randomized control trial in which two groups one is intervention and the other is controlled group .Patient in the Intervention group will be treated with routine pysical therapy, Inspiratory muscle training and early ambulation after surgery, whereas patients in the control group will be not be treated with these interventions and will rather undergo routine physical therapy (ankle pumps, hand pumps isometrics of upper and lower limbs).

Patients in the intervention group will receive treatment until discharge from hospital. On the day of discharge they will be assessed using 6 minute walk test, Borg rate of perceive exertion and health related quality of life scale. Data will be analyzed using SPSS 25.

Study Timeline

• Study First Submitted: 2023-06-14
• Study Start: 2023-06-15
• Study First Submitted QC: 2023-07-07
• Study First Posted: 2023-07-10
• Primary Completion: 2023-08-15
• Study Completion: 2023-11-20
• Status Verified: 2024-06
• Last Update Submitted: 2024-06-11
• Last Update Posted: 2024-06-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 46

Inclusion Criteria

• Both Gender patients
• Patients who agreed to participate
• Age: 35 to 55

Exclusion Criteria

• Patients with history of Angioplasty or CABG
• Chronic Renal failure
• Cardiac arrhythmias
• History of stroke
• Unstable angina

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Inspiratory muscle training and early ambulation	Inspiratory muscle training	Intervention group will be treated with Inspiratory muscle training once in a week for at least 3 weeks
physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs.	physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs.	Control group routine physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs once in a week for at least 3 weeks

Primary Outcome Measures

Name	Time	Method
6 Min walk test	4 weeks	The 6 min walk test is a sub-maximal exercise test used to assess aerobic capacity and endurance.It is also use to monitor your response to treatments for heart lung and other health problems.Provides a measure for integrated global response of multiple cardiopulmonary and musculoskeletal systems involved in exercise.

Secondary Outcome Measures

Name	Time	Method
Spirometer:	4 weeks	A spirometer is used to measure pulmonary function test including FVC, FEV1 and FEV1/FVC ratio. The normal values of FEV1/FVC ratio are \>0.70 and FVC, FEV1 are \>80% of predicted age

Trial Locations

Locations (1)

National hospital Lahore.; 🇵🇰 Lahore, Punjab, Pakistan