Comparitive Effects of Elliptical Training vs Resistance Training on Cardiopulmonary Parameters in Post CABG Patients
NCT ID: NCT06656117
Last Updated: 2024-10-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
NA
44 participants
INTERVENTIONAL
2024-04-15
2025-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Elliptical Training Versus Ergo-meter on Cardiopulmonary Parameters in Post CABG Patients
NCT04615481
Effects of Conditioning Exercises and Resistance Interval Training on Post CABG Patients.
NCT06844591
Group-based Cardiac Rehabilitation on Patients With Coronary Artery Bypass Graft Surgery
NCT06317376
Prehabilitation and Coronary Artery Bypass Grafting
NCT04993976
Power Walking On Quality Of Life In Post CABG Patient Undergoing Phase 2 Cardiac Rehabilitation
NCT05706961
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
. 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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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.
Elliptical training
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
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.
Resistance training
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Elliptical training
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
Resistance training
• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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.
45 Years
55 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Riphah International University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sumera Hameed, M.PHIL
Role: PRINCIPAL_INVESTIGATOR
Riphah International University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sehat medical complex
Sialkot, Punjab Province, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
52187 Hamna
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.