Coronary Artery Bypass Graft CABGNCT06656117
Comparitive Effects of Elliptical Training vs Resistance Training on Cardiopulmonary Parameters in Post CABG Patients
A study testing Elliptical training and Resistance training in people with Coronary Artery Bypass Graft CABG, run by Riphah International University at 1 site in Pakistan.
Trial summary
COMPARATIVE EFFECTS OF ELLIPTICAL TRAINING VS RESISTANCE TRAINING ON CARDIOPULMONARY PARAMETERS IN POST CABG PATIENTS Read more about this study
- Who is it for?
- Ages 45 to 55 years
- Conditions the study is for
- Coronary Artery Bypass Graft CABG
- What is being tested?
- Elliptical training and Resistance training
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 44 participants
- Where
- 1 sitePakistan
- Study dates
- 15 Apr 2024to Jan 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 45 to 55 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- 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 .
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country.
About this study
COMPARATIVE EFFECTS OF ELLIPTICAL TRAINING VS RESISTANCE TRAINING ON CARDIOPULMONARY PARAMETERS IN POST CABG PATIENTS
Read the 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.
- Conditions
- Coronary Artery Bypass Graft CABG
- Being tested
- Elliptical training, Resistance training
- Keywords
- CABG, Elliptical training, Resistance training
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Elliptical trainingOther
- Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
Resistance trainingOther
- Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs.
| Study group | Role | What they receive |
|---|---|---|
| Elliptical training | Experimental | * 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. Receives: Other: Elliptical training |
| Resistance training | Experimental | * 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. Receives: Other: Resistance training |
What is being measured
The primary outcome is the main question the study is designed to answer.
modified borg dyspnea scale
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 .
Measured: 4 weeks
Health related quality of life(SF12)
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 .
Measured: 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Oct 2024
- Study start15 Apr 2024
- Primary completion15 Dec 2024 (estimated)
- Study completionJan 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Coronary Artery Bypass Graft CABGStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- In this parallel-group randmoized control trial (RCT),post Cabag patients will br assigned to either elliptical training group or to resistance training group .This study aims to evualate the comparative effects of eliptical training vs resistance training on cardiopulmonary parameters
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 44 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Sumera Hameed, M.PHIL, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06656117
- Sponsor's protocol ID
- 52187 Hamna
- Status last verified
- Oct 2024
- First submitted
- 23 Oct 2024
- Last updated
- 28 Oct 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparitive Effects of Elliptical Training vs Resistance Training on Cardiopulmonary Parameters in Post CABG Patients
- ClinicalTrials.gov ID
- NCT06656117
- Acronym / sponsor ID
- 52187 Hamna
- Conditions
- Coronary Artery Bypass Graft CABG
- Keywords
- CABG, Elliptical training, Resistance training
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 44 participants (estimated)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 15 Apr 2024 (actual)
- Primary completion
- 15 Dec 2024 (estimated)
- Study completion
- Jan 2025 (estimated)
- First posted
- 24 Oct 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
COMPARATIVE EFFECTS OF ELLIPTICAL TRAINING VS RESISTANCE TRAINING ON CARDIOPULMONARY PARAMETERS IN POST CABG PATIENTS
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 design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- In this parallel-group randmoized control trial (RCT),post Cabag patients will br assigned to either elliptical training group or to resistance training group .This study aims to evualate the comparative effects of eliptical training vs resistance training on cardiopulmonary parameters
| Arm | Type | Receives |
|---|---|---|
| Elliptical training | Experimental | Other: 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. |
| Resistance training | Experimental | Other: 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. |
Who may qualify
- Ages
- 45 to 55 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- 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 .
Key exclusion criteria (6 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Elliptical training• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs. | Other | Elliptical training |
| Resistance training• Throughout the training, participants' heart rates were monitored, and they were asked to report any discomfort or unusual signs. | Other | Resistance training |
Primary outcome
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 .
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 .
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2024.
- Individual participant dataSharing planned: No
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Coronary Artery Bypass Graft (CABG)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sumera Hameed, M.PHIL principal investigator
Riphah International University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Elliptical training and Resistance training in people with Coronary Artery Bypass Graft CABG, run by Riphah International University at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 28 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
modified borg dyspnea scale (time frame: 4 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2024.