Clinical application of a wearable integrated volitional control electrical stimulation device for patient with motor disability in upper extremity at subacute phase.

Clinical application of a wearable integrated volitional control electrical stimulation device for patient with motor disability in upper extremity at subacute phase. - Clinical application of a WIVES device for patient with motor disability in upper extremity at subacute phase.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000026624

Enrollment

Registered

2017-04-01

Start date

2017-04-01

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

Stroke, Traumatic brain injury, spinal cord injury, peripheral nerve injury

Interventions

The intervention group attaches a wearable integrated volitional control electrical stimulation device for 6 hours a day, 28 days. The target muscle is extensor digitorum muscle. The patient actively

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria is as following: 1)the patient with motor disability in upper extremity, 2)Those who passed within 180 days since onset, 3) It is possible to detect the electromyogram of finger extension using the integrated volitional control electrical stimulation device.

Exclusion criteria

Exclusion criteria: Exclusion criteria is as following: 1) severe limited range of motion in wrist, 2) severe sensory disturbance , 3) severe higher brain dysfunction, 4) patients with the contraindication of electrical stimulation therapy (Cardiovascular disease, Inserting a metal into the body like a pace maker, Infection, Abnormal blood pressure, Parts of abnormal skin, acute disease, Blood flow disturbance)

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer assessment score for upper extremity	—

Countries

Japan

Contacts

Public ContactSuzuyo Ohashi

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

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

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026