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Factors related to the outcome of Integrated Volitional controlled Electrical Stimulation (IVES) therapy for chronic stroke

Factors related to the outcome of Integrated Volitional controlled Electrical Stimulation (IVES) therapy for chronic stroke - IVES therapy for chronic stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021912
Enrollment
200
Registered
2016-05-01
Start date
2016-05-01
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

Interventions

To encourage the use of the paretic limbs during daily life and daily occupational therapy with IVES for 21 days.

Sponsors

Keio Univ sch. med
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with hemiparesis dues to stroke 2. at least 6 month after the stroke 3. Able to understand and consent the objective and method of the study 4. SIAS knee-mouth test >= 2 5. SIAS finger test < 3 6. Passive range of finger extention > 0 degree 7. Muscle contraction is detectable from the extensor digitrum communis or extensor pollicis longus 8. Independent ambulatory ability with/without walking aids 9. Independent ADL ability with/without functional aids

Exclusion criteria

Exclusion criteria: Contraindication for physical therapy and/or electorical stimulation

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer asseesment for upper extremities, and WMFT testings at just after and 3 month after the end of intervention.

Countries

Japan

Contacts

Public ContactSyoichi Tashiro

Keio Univ sch. med Dept. Rehabilitation Med

s-tashiro@umin.net+81-3-5363-3833

Outcome results

None listed

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