Comparitive Effects of Elliptical Training vs Resistance Training on Cardiopulmonary Parameters in Post CABG Patients

October 24, 2024 updated by: Riphah International University
COMPARATIVE EFFECTS OF ELLIPTICAL TRAINING VS RESISTANCE TRAINING ON CARDIOPULMONARY PARAMETERS IN POST CABG PATIENTS

Study Overview

Status

Enrolling by invitation

Detailed Description

Coronary artery bypass grafting (CABG) has been widely and increasingly used since the 1960s as a common surgical procedure to restore blood flow into the stenotic coronary arteries

. It is one of the effective ways to treat coronary artery disease, which can significantly relieve patients' myocardial ischemia and hypoxia symptoms and improve their quality of life.

Data were collected from Itefaq hospital, sehat medical complex Lahore. Borg dyspnea and quality of life (SF12) questioner were used before and after the intervention.

Assessment was done through the tool before and after the treatment.

Study Type

Interventional

Enrollment (Estimated)

44

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Sialkot, Punjab, Pakistan, 51310
        • Sehat Medical Complex

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Both male and female age 45-55 years.
  • Post Coronary Artery Bypass Grafting (CABG) patients at phase III cardiac rehabilitation were included .
  • Patients who had physically active lower limbs were included .

Exclusion Criteria:

  • Participants who had psychological conditions that may influence understanding or answering of questionnaire.
  • Patients with other cardiac lesions combined with simultaneous surgical management, such as valvular lesions, macro vascular lesions, and ventricular wall tumors.
  • Patients diagnosed with emergency CABG, minimally invasive CABG, or recurrent cardiac surgery.
  • Patients with severe dysfunction of important organs such as the lung, liver, and kidney.
  • Patients with recent major surgery or trauma of other parts of body.
  • Pregnant or lactating women.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Elliptical training
  • Patients in group A started with a five-minute warm-up, which included cycling on a Star Trac bike and dynamic stretching.
  • Following the warm-up, participants were instructed to perform Elliptical training after completing breathing exercises.
  • At the end of the training session, participants from both groups engaged in a five-minute gradual cool down.
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
Experimental: Resistance training
  • Patients in group B started with a five-minute warm-up, which included cycling on a Star Trac bike and dynamic stretching.
  • Following the warm-up, participants were instructed to perform Resistance training after completing breathing exercises.
  • At the end of the training session, participants from both groups engaged in a five-minute gradual cool down.
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
modified borg dyspnea scale
Time Frame: 4 weeks
The modified Borg dyspnea score is a version of the CR10; 45 it uses a scale from 0 to 10, where 0 represents no dyspnea and 10 represents maximal dyspnea. Scores are obtained at the end of the 6MWD test and reflect the maximum degree of dyspnea at any time during the walk test .
4 weeks
Health related quality of life(SF12)
Time Frame: 4 weeks
The SF-12 Health version 2 is a generic short form health survey developed in the USA from the original SF-36. It produces two summary measures evaluating physical and mental self-perceived health; for this reason, it could be a suitable and complete tool to assess the self-perceived quality of life of university students because it allows investigating both the aspects .
4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sumera Hameed, M.PHIL, Riphah International University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 15, 2024

Primary Completion (Estimated)

December 15, 2024

Study Completion (Estimated)

January 1, 2025

Study Registration Dates

First Submitted

October 23, 2024

First Submitted That Met QC Criteria

October 23, 2024

First Posted (Actual)

October 24, 2024

Study Record Updates

Last Update Posted (Actual)

October 28, 2024

Last Update Submitted That Met QC Criteria

October 24, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 52187 Hamna

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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