Effect of Electrical Stimulation Device for Upper Limb Paralysis

Clinical Evaluation of a Wearable Volitional Movement-Assist Electrical Stimulation Device in Patients with Upper Limb Motor Paralysis - W-VMAF Study (Wearable Volitional Movement-Assist FES Study)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000058764

Enrollment

Registered

2026-02-01

Start date

2026-01-07

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Upper limb paralysis caused by central nervous system diseases such as stroke (cerebral infarction, intracerebral hemorrhage, subarachnoid hemorrhage), head injury, cervical spinal cord injury, cervical spondylotic myelopathy, and syringomyelia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Age >= 20 years at the time of consent. 2.No restriction on sex.

Exclusion criteria

Exclusion criteria: 1. Patients who were unable to complete the self-directed training program. 2. Patients with missing outcome assessments.

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer Assessment (Upper Extremity section)	—

Secondary

Measure	Time frame
MAL, WMFT, ARAT, MAS, device wearing time and usability evaluation	—

Countries

Japan

Contacts

Public ContactNorikazu Hishikawa

Graduate School of Medical Science, Kyoto Prefectural University of Medicine Department of Rehabilitation Medicine

hisikawa@koto.kpu-m.ac.jp075-251-5324

Outcome results