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Repetitive Peripheral Magnetic Stimulation (rPMS) for Post-Stroke Sequelae: A Prospective Interventional Study

Repetitive Peripheral Magnetic Stimulation (rPMS) for Post-Stroke Sequelae: A Prospective Interventional Study - rPMS-PSS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060037
Enrollment
50
Registered
2025-12-10
Start date
2024-08-01
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

Patients presenting with post-stroke sequelae such as dysphagia, gait disturbance, upper-limb dysfunction, and respiratory impairment.

Interventions

rPMS combined with intensive rehabilitation program

Sponsors

Jikei University School of Medicine
Lead Sponsor
Koyama Rehabilitation Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with post-stroke symptoms such as dysphagia, walking disorder, upper limb dysfunction, and respiratory dysfunction

Exclusion criteria

Exclusion criteria: Patients who are unable to fully understand the study content due to impaired comprehension or other reasons will be excluded from the study. Patients with internal medical devices (such as pacemakers), internal metal objects (such as implants) near the magnetic stimulation site, patients with serious heart disease, or patients with venous thrombosis will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
(For upper limb function) Fugl-Meyer Assessment for the Upper Extremity (FMA-UE) Action Research Arm Test (ARAT) Modified Ashworth Scale Active range of motion (AROM)

Countries

Japan

Contacts

Public ContactShoji Kinoshita

Jikei University School of Medicine Department of Rehabilitation Medicine

kinoshita@jikei.ac.jp03-3433-1111

Outcome results

None listed

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