- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06656117
Comparitive Effects of Elliptical Training vs Resistance Training on Cardiopulmonary Parameters in Post CABG Patients
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Sialkot, Punjab, Pakistan, 51310
- Sehat Medical Complex
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
|
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
|
|
Experimental: Resistance training
|
• 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
Sponsor
Investigators
- Principal Investigator: Sumera Hameed, M.PHIL, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 52187 Hamna
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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