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

NCT ID: NCT06317376

Last Updated: 2024-03-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

54 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-01

Study Completion Date

2024-01-18

Brief Summary

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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.

Detailed Description

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Conditions

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Post-cardiac Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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experimental group (MICT)

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

Group Type EXPERIMENTAL

MICT with Aerobic exercise on treadmill

Intervention Type OTHER

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

control group (standard protocol)

Perform standard hospital protocol 2-3 session per week

Group Type OTHER

standard hospital protocol

Intervention Type OTHER

standard hospital protocol

Interventions

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MICT with Aerobic exercise on treadmill

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

Intervention Type OTHER

standard hospital protocol

standard hospital protocol

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

40 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Riphah International University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Maria Razzaq, MS

Role: PRINCIPAL_INVESTIGATOR

Riphah International University

Locations

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RMI

Peshawar, , Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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REC/014131 Maria Haseen

Identifier Type: -

Identifier Source: org_study_id

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