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

Riphah International University46 enrolled

Overview

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.

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 Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Exercise

Interventions

Inspiratory muscle trainingOTHER

Group A: Intervention group will be treated with Inspiratory muscle training and early ambulation and routine physical therapy including ankle pumps,hand pumps isometrics of upper and lower limbs after surgery

physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs.OTHER

Group B: Control group routine physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs

Eligibility

Sex: ALLMin age: 35 YearsMax age: 55 Years

Medical Language ↔ Plain English

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

Locations (1)

National hospital Lahore.

Lahore, Punjab Province, Pakistan

Outcomes

Primary Outcomes

6 Min walk test

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.

Time frame: 4 weeks

Secondary Outcomes

Spirometer:

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

Time frame: 4 weeks

Data from ClinicalTrials.gov

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