Effects of IMT ON Dyspnea, PF and Quality of Life in Patients With CABG
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 46
- Locations
- 1
- Primary Endpoint
- 6 Min walk test
Study Overview
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 Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Masking 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.
Eligibility Criteria
- Ages
- 35 Years to 55 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Arms & Interventions
Inspiratory muscle training and early ambulation
Intervention group will be treated with Inspiratory muscle training once in a week for at least 3 weeks
Intervention: Inspiratory muscle training (Other)
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
Intervention: physical therapy including ankle pumps, hand pumps isometrics of upper and lower limbs. (Other)
Outcomes
Primary Outcomes
6 Min walk test
Time Frame: 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 Outcomes
- Spirometer:(4 weeks)