Study of Phase I Cardiac Rehabilitation Using an Upper Limb Cycle Ergometer After Coronary Artery Bypass Surgery
Led by Riphah International University · Updated on 2025-08-19
44
Participants Needed
1
Research Sites
4 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are studying the effects of using an upper limb cycle ergometer during phase I cardiac rehabilitation in patients who have undergone coronary artery bypass grafting CABG. The goal is to see if this arm ergometer exercise can improve quality of life, reduce breathlessness, enhance functional abilities, support cardiovascular health, and improve upper limb mobility. The study aims to reduce complications after surgery, lower healthcare costs, and improve patient care.
Participants will be randomly assigned to one of two groups. Group A will perform upper limb exercises on the arm ergometer for 5 minutes at 30 rotations per minute, three times daily for 7 days, along with standard cardiac rehabilitation treatments such as breathing exercises, active upper and lower limb exercises, ambulation, and sitting transfers. Group B will receive the same standard treatments but without the arm ergometer exercises. The study will last ten months and focus on the immediate post-operative period after CABG.
During the study, patients will be evaluated after one week using questionnaires and scales that assess their functional independence, quality of life, and breathlessness. Researchers will also monitor heart rate, respiratory rate, blood pressure, and oxygen levels daily for seven days. Data will be analyzed to compare the effects of adding the arm ergometer to standard rehabilitation. This trial is designed to provide detailed insight into recovery progress and the impact of the arm ergometer on post-surgery outcomes.
CONDITIONS
Brief Title
Effect of Phase I Cardiac Rehab With or Without Upper Limb Cycle Ergometer
Research Team
I
imran amjad, Phd
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Patients with pulmonary diseases or thyroid disorders
Mechanical ventilation for more than 24 hours
Mean arterial pressure below 60 mmHg or above 140 mmHg
Heart rate exceeding 120 beats per minute
Orthopedic conditions preventing use of upper and lower limbs
Neurological impairments affecting breathing or heart rate
Intra-aortic balloon implantation during surgery
Postoperative complications such as pulmonary embolism
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - 7 days
Participants receive phase I cardiac rehabilitation after coronary artery bypass grafting (CABG). Group A performs upper limb exercise on an arm ergometer 3 times daily for 7 days along with standard breathing and physical exercises. Group B receives the same standard exercises without the arm ergometer. Activities include breathing exercises, active upper and lower limb exercises, ambulation within inpatient wards, and sitting transfer, all progressing as tolerated.
Daily sessions for 7 days (inpatient)
Follow-up
Duration - 1 day
Participants are evaluated after one week of rehabilitation to assess quality of life, dyspnea, functional independence, and cardiovascular parameters.
1 visit (in-person) after 7 days
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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