CABGNCT07331584
Elastic Band Versus Free Weight Resistance Training in Phase 2 of CABG Patients.
A study testing dumbell and thera band in people with CABG, run by Riphah International University at 1 site in Pakistan.
Trial summary
The aim of this study compares the effects of elastic band and free weights on functional capacity, lung function and quality of life in phase 2 coronary artery bypass grafting patients. Resistance training is vital in cardiac rehabilitation for improving physical function, strength, and independence. Read more about this study
- Who is it for?
- Ages 45 to 65 years
- Conditions the study is for
- CABG
- What is being tested?
- dumbell and thera band
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 42 participants
- Where
- 1 sitePakistan
- Study dates
- 17 Apr 2025to 17 Dec 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 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male and female
- Age (45-64)
- Stable cardio vascular status
- Able to participate in mild to moderate exercise
- Must be in 4-8 week of CABG and medically cleared for phase 2.
- Able to provide informed consent
Who cannot join
- Unstable cardiovascular condition.
- Pulmonary conditions
- Cognitive impairment
- Other major surgeries and comorbidities
Trial locations and contacts
1 site in 1 country.
Pakistan1 site
Sehat Medical Complex Hanjerwal
Lahore, Punjab Province, 42000
About this study
Official title: Effects of Elastic Band Versus Free Weight Resistance Training on Functional Capacity, Pulmonary Functioning and Quality of Life in Phase 2 of CABG Patients.
The aim of this study compares the effects of elastic band and free weights on functional capacity, lung function and quality of life in phase 2 coronary artery bypass grafting patients. Resistance training is vital in cardiac rehabilitation for improving physical function, strength, and independence. These patients typically experience reduced functional capacity and lung function due to post-surgical deconditioning and inactivity, which can also impact quality of life.Determining whether elastic bands or free weights provide greater benefits in these areas may help optimize cardiac rehabilitation protocols by identifying a safe, effective, and accessible approach for improving patient outcomes. This research has the potential to guide evidence-based resistance training in post- coronary artery bypass grafting rehabilitation, ultimately supporting recovery and enhancing quality of life of patients.
Read the detailed description
Patients who undergo cardiac surgery frequently faces pulmonary complications. This study aims to compare the effects of elastic band and free weights on functional capacity, lung function and quality of life in phase 2 coronary artery bypass grafting patients. Resistance training is vital in cardiac rehabilitation for improving physical function, strength, and independence. These patients typically experience reduced functional capacity and lung function due to post-surgical deconditioning and inactivity, which can also impact quality of life. Determining whether elastic bands or free weights provide greater benefits in these areas may help optimize cardiac rehabilitation protocols by identifying a safe, effective, and accessible approach for improving patient outcomes.
This research has the potential to guide evidence-based resistance training in post- coronary artery bypass grafting rehabilitation, ultimately supporting recovery and enhancing quality of life of patients. By comparing the effects of elastic band versus free weights resistance training on functional capacity, pulmonary functioning and quality of life in phase 2 of coronary artery bypass grafting. It will be a randomized clinical trial. Age of selected patients will be between 45 to 65 years and data will be collected from them. There will be two groups i.e. group A will receive 10 min walk warm up after that resistance training of upper and lower limb by using dumb bells and group B will receive 10 min of walk as warm up after that resistance training of upper and lower limb by using elastic band. International physical activity questionnaire used for quality of life, 6 min walk test for functional capacity and forced expiratory volume, forced vital capacity and peak expiratory flow rate for lung functioning.
Trial will be completed in 12 weeks (2x/week) after patients got discharged 4-8 weeks after the surgery and before and after each session, primary and secondary outcomes will be measured for both groups. After data collection, data will be analyzed using SPSS version 25
- Conditions
- CABG
- Being tested
- dumbell, thera band
- Keywords
- coronary artery bypass graft, resistance training, functional residual capacities, pulmonary function test, quality of life
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
dumbellOther
Group A will receive the exercises from dumb bells we will focus on both upper limb and lower limb the total session would be of 20-30 minutes, will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) and after that 5-7 min of cool down. Dyspnea will be measured.
thera bandOther
Group B will receive the exercise form elastic band (TheraBand) for both upper limb and lower limb. Total session time would be 30 minutes will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) 10-12 reps and 1 set in starting progressively increased to 3 reps after that at the end of session 5-7 min cool down and gentle stretching 2 times per week for 12 weeks. Dyspnea should be monitored.
| Study group | Role | What they receive |
|---|---|---|
| Dumbell | Experimental | Group A will receive the exercises from dumb bells we will focus on both upper limb and lower limb the total session would be of 20-30 minutes, will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) and after that 5-7 min of cool down. Dyspnea will be measured. Receives: Other: dumbell; Other: thera band |
| elastic band | Experimental | Group B will receive the exercise form elastic band (TheraBand) for both upper limb and lower limb. Total session time would be 30 minutes will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) 10-12 reps and 1 set in starting progressively increased to 3 reps after that at the end of session 5-7 min cool down and gentle stretching 2 times per week for 12 weeks. Dyspnea should be monitored. Receives: Other: dumbell; Other: thera band |
What is being measured
The primary outcome is the main question the study is designed to answer.
Forced Expiratory Volume in 1 Second
Forced Expiratory Volume in 1 Second (FEV1) is a key lung function test measuring how much air you can forcefully blow out in the first second of a deep breath, indicating how quickly your airways empty.
Measured: 12 weeks
international physical activity questionnaire : Quality of life
The international physical activity questionnaire is a widely used tool designed to assess physical activity levels among adults. It evaluates various types of activity, including walking, moderateintensity activities, and vigorous-intensity activities, over the past week. The International Physical Activity Questionnaire (IPAQ) scoring involves converting reported activity (walking, moderate, vigorous) into MET-minutes per week by multiplying minutes by MET values (3.3 for walking, 4 for moderate, 8 for vigorous). Scores are then categorized as Low, Moderate, or High, based on specific criteria like achieving ≥3000 MET-min/week (High) or meeting minimum days/minutes for moderate activity (e.g., ≥3 days vigorous or ≥5 days moderate/walking for Moderate), to assess overall activity levels.
Measured: 12 week
6 Minute Walk Test
A 6 min walk test is easier, safer to administer, better tolerated and better reflects activity of daily Living than another walk test. The 6-Minute Walk Test (6MWT) scoring primarily focuses on the total distance walked (6MWD) in meters, calculated by counting laps and adding any partial lap, noting rest times. Scores are interpreted using age/sex/height/weight-specific prediction equations (like those from the American Thoracic Society) to compare actual distance to expected normal, with lower scores indicating poorer function, though the longest distance from multiple tests is used to account for learning effects.
Measured: 12 weeks
Forced Vital Capacity
FVC, or Forced Vital Capacity, is a key measurement in spirometry (lung function tests) that quantifies the total amount of air you can forcefully exhale from your lungs after taking the deepest breath
Measured: 12 week
Peak Expiratory Flow Rate
Peak Expiratory Flow Rate (PEFR) measures the fastest speed you can forcefully exhale air from your lungs
Measured: 12 Week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jan 2026
- Study start17 Apr 2025
- Primary completion17 Dec 2025
- Study completion17 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for 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
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 42 participants (actual)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Riffat Malik, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07331584
- Sponsor's protocol ID
- Fatima Shoaib
- Status last verified
- Dec 2025
- First submitted
- 29 Dec 2025
- Last updated
- 12 Jan 2026
- 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 12 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Elastic Band Versus Free Weight Resistance Training on Functional Capacity, Pulmonary Functioning and Quality of Life in Phase 2 of CABG Patients.
- ClinicalTrials.gov ID
- NCT07331584
- Acronym / sponsor ID
- Fatima Shoaib
- Conditions
- CABG
- Keywords
- coronary artery bypass graft, resistance training, functional residual capacities, pulmonary function test, quality of life
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 42 participants (actual)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 17 Apr 2025 (actual)
- Primary completion
- 17 Dec 2025 (actual)
- Study completion
- 17 Dec 2025 (actual)
- First posted
- 12 Jan 2026 (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.
The aim of this study compares the effects of elastic band and free weights on functional capacity, lung function and quality of life in phase 2 coronary artery bypass grafting patients. Resistance training is vital in cardiac rehabilitation for improving physical function, strength, and independence. These patients typically experience reduced functional capacity and lung function due to post-surgical deconditioning and inactivity, which can also impact quality of life.Determining whether elastic bands or free weights provide greater benefits in these areas may help optimize cardiac rehabilitation protocols by identifying a safe, effective, and accessible approach for improving patient outcomes. This research has the potential to guide evidence-based resistance training in post- coronary artery bypass grafting rehabilitation, ultimately supporting recovery and enhancing quality of life of patients.
Detailed description
Patients who undergo cardiac surgery frequently faces pulmonary complications. This study aims to compare the effects of elastic band and free weights on functional capacity, lung function and quality of life in phase 2 coronary artery bypass grafting patients. Resistance training is vital in cardiac rehabilitation for improving physical function, strength, and independence. These patients typically experience reduced functional capacity and lung function due to post-surgical deconditioning and inactivity, which can also impact quality of life. Determining whether elastic bands or free weights provide greater benefits in these areas may help optimize cardiac rehabilitation protocols by identifying a safe, effective, and accessible approach for improving patient outcomes.
This research has the potential to guide evidence-based resistance training in post- coronary artery bypass grafting rehabilitation, ultimately supporting recovery and enhancing quality of life of patients. By comparing the effects of elastic band versus free weights resistance training on functional capacity, pulmonary functioning and quality of life in phase 2 of coronary artery bypass grafting. It will be a randomized clinical trial. Age of selected patients will be between 45 to 65 years and data will be collected from them. There will be two groups i.e. group A will receive 10 min walk warm up after that resistance training of upper and lower limb by using dumb bells and group B will receive 10 min of walk as warm up after that resistance training of upper and lower limb by using elastic band. International physical activity questionnaire used for quality of life, 6 min walk test for functional capacity and forced expiratory volume, forced vital capacity and peak expiratory flow rate for lung functioning.
Trial will be completed in 12 weeks (2x/week) after patients got discharged 4-8 weeks after the surgery and before and after each session, primary and secondary outcomes will be measured for both groups. After data collection, data will be analyzed using SPSS version 25
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Dumbell | Experimental | Other: dumbell, Other: thera bandGroup A will receive the exercises from dumb bells we will focus on both upper limb and lower limb the total session would be of 20-30 minutes, will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) and after that 5-7 min of cool down. Dyspnea will be measured. |
| elastic band | Experimental | Other: dumbell, Other: thera bandGroup B will receive the exercise form elastic band (TheraBand) for both upper limb and lower limb. Total session time would be 30 minutes will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) 10-12 reps and 1 set in starting progressively increased to 3 reps after that at the end of session 5-7 min cool down and gentle stretching 2 times per week for 12 weeks. Dyspnea should be monitored. |
Who may qualify
- Ages
- 45 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Male and female
- Age (45-64)
- Stable cardio vascular status
- Able to participate in mild to moderate exercise
- Must be in 4-8 week of CABG and medically cleared for phase 2.
Key exclusion criteria (4 listed)
- Unstable cardiovascular condition.
- Pulmonary conditions
- Cognitive impairment
- Other major surgeries and comorbidities
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 |
|---|---|---|
| dumbellGroup A will receive the exercises from dumb bells we will focus on both upper limb and lower limb the total session would be of 20-30 minutes, will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) and after that 5-7 min of cool down. Dyspnea will be measured. | Other | Dumbell, elastic band |
| thera bandGroup B will receive the exercise form elastic band (TheraBand) for both upper limb and lower limb. Total session time would be 30 minutes will be focusing on chest (pectoralis major), back (latissimus dorsi, rhomboids), legs (quadriceps, hamstring, glutes) and core (abdominals, lower back) 10-12 reps and 1 set in starting progressively increased to 3 reps after that at the end of session 5-7 min cool down and gentle stretching 2 times per week for 12 weeks. Dyspnea should be monitored. | Other | Dumbell, elastic band |
Primary outcome
Forced Expiratory Volume in 1 Second
Time frame: 12 weeks
Forced Expiratory Volume in 1 Second (FEV1) is a key lung function test measuring how much air you can forcefully blow out in the first second of a deep breath, indicating how quickly your airways empty.
international physical activity questionnaire : Quality of life
Time frame: 12 week
The international physical activity questionnaire is a widely used tool designed to assess physical activity levels among adults. It evaluates various types of activity, including walking, moderateintensity activities, and vigorous-intensity activities, over the past week. The International Physical Activity Questionnaire (IPAQ) scoring involves converting reported activity (walking, moderate, vigorous) into MET-minutes per week by multiplying minutes by MET values (3.3 for walking, 4 for moderate, 8 for vigorous). Scores are then categorized as Low, Moderate, or High, based on specific criteria like achieving ≥3000 MET-min/week (High) or meeting minimum days/minutes for moderate activity (e.g., ≥3 days vigorous or ≥5 days moderate/walking for Moderate), to assess overall activity levels.
6 Minute Walk Test
Time frame: 12 weeks
A 6 min walk test is easier, safer to administer, better tolerated and better reflects activity of daily Living than another walk test. The 6-Minute Walk Test (6MWT) scoring primarily focuses on the total distance walked (6MWD) in meters, calculated by counting laps and adding any partial lap, noting rest times. Scores are interpreted using age/sex/height/weight-specific prediction equations (like those from the American Thoracic Society) to compare actual distance to expected normal, with lower scores indicating poorer function, though the longest distance from multiple tests is used to account for learning effects.
Forced Vital Capacity
Time frame: 12 week
FVC, or Forced Vital Capacity, is a key measurement in spirometry (lung function tests) that quantifies the total amount of air you can forcefully exhale from your lungs after taking the deepest breath
Peak Expiratory Flow Rate
Time frame: 12 Week
Peak Expiratory Flow Rate (PEFR) measures the fastest speed you can forcefully exhale air from your lungs
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Jan 2026.
- Individual participant dataSharing planned: No
Related trials for CABG
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Thiamine Intervention and Coronary Artery Bypass Grafting
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Not yet recruitingObservational study
Preoperative Gastric Ultrasound and Anaesthetic Management in Patients Undergoing Coronary Artery Bypass Grafting
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Investigation of the Effects of Respiratory Muscle Training Combined With Otago Exercises in Elderly Patients Undergoing Coronary Artery Bypass Graft Surgery
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.
Riffat Malik 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 dumbell and thera band in people with 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 6 inclusion and 4 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: finished, as of the sponsor's last update on 12 Jan 2026. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Forced Expiratory Volume in 1 Second (time frame: 12 weeks). The study lists 5 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 12 Jan 2026.