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Verification of the effectiveness of combined therapy of exercise therapy and repetitive peripheral magnetic stimulation (rPMS) for improving lower limb function and movement in convalescent stroke patients; randomized crossover trial

Verification of the effectiveness of combined therapy of exercise therapy and repetitive peripheral magnetic stimulation (rPMS) for improving lower limb function and movement in convalescent stroke patients; randomized crossover trial - stroke rPMS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060662
Enrollment
20
Registered
2026-02-15
Start date
2026-01-18
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

Patients aged 40 or older to younger than 65 Patients admitted to our hospital&#39

Interventions

Conventional rehabilitation and rPMS combination program Conventional rehabilitation

Sponsors

others
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients aged 40 or older to younger than 65 Patients admitted to our hospital's rehabilitation ward for rehabilitation treatment within 60 days of stroke onset Patients who have had a first stroke and the type of stroke is unilateral cerebral infarction or cerebral hemorrhage Patients with mild to moderate lower limb motor paralysis (Brunnstrom stage 3 to 5) Patients with a degree of gait disorder with a Functional Ambulation Categories (FAC) score of 3 to 4

Exclusion criteria

Exclusion criteria: Patients with metal implants or implant devices (e.g. cardiac pacemaker) within the stimulation site Pregnant patients Patients with or history of epilepsy Patients whose general conditions such as blood pressure, pulse rate, and blood sugar levels are unstable due to dyspnea on exertion, heart failure, arrhythmia, myocardial infarction, etc., and who are judged to have difficulty in functional training. Patients with a history of neurological diseases or orthopedic diseases that affect trunk and lower extremity function *Patients with comorbid diseases such as degenerative diseases, scoliosis, osteoporosis, etc. whose symptoms are judged to be aggravated by functional training Patients with subarachnoid hemorrhage, severe liver disorder, renal disorder, or cardiovascular disease Patients with higher brain dysfunction such as severe sensory impairment, ataxia, or aphasia Patients who do not have the capacity to consent themselves as research subjects Patients whose attending physician has determined that they are unable to participate in this study, taking into account their general condition.

Design outcomes

Primary

MeasureTime frame
Manual muscle strength testing using a handheld dynamometer (HHD)

Secondary

MeasureTime frame
Functional Independence Measure(FIM)

Countries

Japan

Contacts

Public Contactkenji yoshida

3-3-9 Ishimaru, Nishi-ku, Fukuoka City, Fukuoka Prefecture rehabilitation department

pt.yoshida.hakujyuji@gmail.com092-891-2611

Outcome results

None listed

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