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The effects of repetitive peripheral magnetic stimulation in patient with spastic hemiparesis after stroke: A randomized-controlled study

The effects of repetitive peripheral magnetic stimulation in patient with spastic hemiparesis after stroke: A randomized-controlled study - REPMAST

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00007899
Enrollment
80
Registered
2015-03-24
Start date
2015-04-15
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

I60-I69 G81.1

Interventions

Group 1: repetitive peripheral magnetic stimulation (rPMS) (interventiongroup): The stimulation is 15 minutes daily for three weeks with a total of 15 sessions. The stimulation intensity is adjusted
The arm is placed to be stimulated or maintained by the therapist magnetic stimulator: Magstim Rapid² Instruction: Patients are asked to relax and observe their arm Group 2: peripheral electrical st

Sponsors

Moritz Klinik Bad Klosterlausnitz
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: subacute stroke (incident not longer than six months back) spastic hemiparesis of the upper limb (at least modified ashworth scale 1) a slight function in the fingers or hand (at least 1 point in the Fugl-Meyer-test in subscore C)

Exclusion criteria

Exclusion criteria: Epilepsy, implantated metal in the stimulation area implantated medical devices dysfunctional speech comprehension pregnancy

Design outcomes

Primary

MeasureTime frame
The primary outcome is the Fugl-Meyer Test of the upper extremity, a test that evaluated the function of the affected upper extremity. This test will be performed directly after the end of the three weeks intervention-/controllintervention.

Secondary

MeasureTime frame
The secondary outcome is determined with a questionnaire, the Katz Index of Independence Activities of daily living (ADL). That questionnaire aims to identify the dependence in the performance in the activities of daily living and will be performed six months after the end of the intervention /controllintervention.

Countries

Germany

Contacts

Public ContactKristin Pohl

Moritz Klinik Bad Klosterlausnitz

kristin.pohl@moritz-klinik.de036601/49418

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026