Skip to content

Development and application of a new device to reduce involuntary arm movements during walking in patients with stroke

Development and application of a novel electromyographic-driven multi-channel functional electrical stimulation for the management of homolateral limb synkinesis during post-stroke gait - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092187
Enrollment
28
Registered
2025-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: I639- Cerebral infarction, unspecified

Interventions

Intervention1: Electromyographic driven multi-channel functional electrical stimulation device: Post-stroke patients with upper limb homolateral limb synkinesis during gait will undergo gait training

Sponsors

Kasturba Medical College Mangalore, MAHE, Manipal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosed sub-acute (15 to 180 days) or chronic (more than 180 days) medically stable post stroke patients 2. Ability to ambulate 10m without assistance 3. HLS in the upper limb with a modal Associated Reaction Rating Scale score of more than or equal to 1

Exclusion criteria

Exclusion criteria: 1. Presence of other neurological or neurobehavioral or orthopedic or cardiopulmonary conditions that could affect upper limb or gait 2. Presence of contracture in the affected upper limb 3. Patients who have received baclofen or botulinum toxin treatment within 3 months prior to the day of screening 4. Patients with cognitive impairments (Saint Louis University Mental Scale less than or equal to 26 in patients with a high school education, and less than or equal to 24 in patients who do not have a high school education) 5. Patients with complete sensory loss in the affected upper limb 6. Any active dermatological conditions that could prevent the placement of the device over the affected upper limbs

Design outcomes

Primary

MeasureTime frame
Surface eletromyography, OpenCap, gyroscopes (two), Associated Reaction Rating Scale Timepoint: 0,4,8,12 weeks

Secondary

MeasureTime frame
Stroke Rehabilitation Assessment of Movement (STREAM), 10m walk testTimepoint: 0,4,8,12 weeks

Countries

India

Contacts

Public ContactDr Abraham M Joshua

Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal

abraham.joshua@manipal.edu9886188221

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026