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Efficiency of Pulsed Electromagnetic Field & Neuromuscular Electrical Stimulation on Hemiplegic Shoulder Pain

Efficiency of Pulsed Electromagnetic Field and Neuromuscular Electrical Stimulation on Painful Shoulder following Stroke - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054354
Enrollment
51
Registered
2023-06-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: I69- Sequelae of cerebrovascular disease

Interventions

Intervention1: Pulsed Electromagnetic Field: Subjects will receive Pulsed Electromagnetic Field (30 minutes) three times a week for six weeks. Intervention2: Neuromuscular Electrical Stimulation: Subj

Sponsors

Guru Jambheshwar University of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Duration of stroke more than 6 months 2.Patient with unilateral hemiplegia 3.Score on Visual Analogue Scale (VAS) more than 4 4.Patient with 1-3 degree of spasticity according to Modified Ashworth Scale (MAS)

Exclusion criteria

Exclusion criteria: 1.Had history of traumatic shoulder injury 2.Uncontrolled seizures 3.Severe arrhythmia 4.History of tuberculosis/ infection in the shoulder 5.Patient with severe spasm or contracture of upper limb 6.Severe cognitive impairment 7.Cardiac pacemaker

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS) Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up)—

Secondary

MeasureTime frame
Active Range of Motion (AROM)Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up);Fugl-Meyer Assessment-Upper Extremity(FMA-UE) Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up);Modified Ashworth Scale(MAS)Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up);Passive Range of Motion(PROM)Timepoint: Outcome measured before the start of intervention(at 0 weeks)and after the completion of treatment(at 6 weeks & follow up)—

Countries

India

Contacts

Public ContactDr Sonu Punia

Guru Jambheshwar University of Science and Technology Hisar

sonu.punianeuropt@gmail.com9466373990

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026