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Comparison of EMG Biofeedback Based Physiotherapy and Standard Cardiac Rehabilitation in Patients Following Heart Bypass Surgery

Effect of EMG Biofeedback Based Neuromuscular Re-education versus Conventional Cardiac Rehabilitation on Pain, Voluntary Muscle Activation, and Functional Recovery in Post-CABG Patients: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102224
Enrollment
46
Registered
2026-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I257- Atherosclerosis of coronary arterybypass graft(s) and coronary artery of transplanted heart with angina pectoris

Interventions

Intervention1: EMG Biofeedback: EMG biofeedback will be used as a neuromuscular re-education tool in addition to routine cardiac rehabilitation. Surface electrodes will be placed over selected upper l

Sponsors

Dr Akshay Singh Parihar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who have undergone coronary artery bypass graft (CABG) surgery. Adults aged 40 70 years. Medically stable and cleared for cardiac rehabilitation. Ability to follow verbal commands and actively participate in physiotherapy. Willingness to provide written informed consent.

Exclusion criteria

Exclusion criteria: Hemodynamically unstable patients. Presence of post-operative complications restricting physiotherapy (e.g., severe arrhythmias, sternal instability). Neurological or musculoskeletal disorders affecting upper limb function. Cognitive impairment limiting understanding of instructions. Patients with implanted electrical devices contraindicating EMG use.

Design outcomes

Primary

MeasureTime frame
6 minute walk test NPRSTimepoint: At baseline and at the end of 2 weeks

Secondary

MeasureTime frame
Chest ExpansionTimepoint: At baseline & at the end of two weeks;Modified Borg ScaleTimepoint: At baseline & at the end of 2 weeks;30-second Sit to Stand TestTimepoint: At baseline & at the end of 2 weeks

Countries

India

Contacts

Public ContactDR AKSHAY SINGH PARIHAR

RJS College of Physiotherapy

kharwandikardivya1632@gmail.com7893466634

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026