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?RTMS effects on PSP patients

Effect of repetitive transcranial magnetic stimulation on dysarthria and postural disturbance in patients with progressive supranuclear palsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230504058069N1
Enrollment
12
Registered
2023-06-18
Start date
2023-05-26
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

PSP Proressive supranuclear palsy. Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]

Interventions

Intervention 1: Intervention group: 6 PSP patients who receive 10 sessions of rTMS with 900 daily pulses of 10 Hz every other day. The location of the coils will be in contact with the skull two centi

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: PSP patients that was diagnosed by national institute of neurologic disease and stroke for PSP citeria patient who can stand alon and without helping patient who can walking at least a few steps without helping patient who can speak and answer the questions patient who has signed the informed consent form to enter the plan

Exclusion criteria

Exclusion criteria: patient who was diagnosed dementia by DSM-IV criteria patient who had vestibular or properioception or sensory deficits patient who has any contraindication of brain stimulation (such as pacemakers or presence of metal objects in the head) the patient had dysartheria before the onset of disease patient who had past medical history of stroke patient who is mute

Design outcomes

Primary

MeasureTime frame
Checking the postural instabilility of patients. Timepoint: The beginning of the study (before starting rTMS), the end of receiving rTMS, four months later. Method of measurement: Kinematic analysis of scoring movement based on the results of forces and energy.;Checking the speech and swalling of patients. Timepoint: The beginning of the study (before starting rTMS), the end of receiving rTMS, four months later. Method of measurement: Wanberg's auditory-perceptual assessment index and the Northwestern swallowing disorder test.

Secondary

MeasureTime frame
????? ????? ???????. Timepoint: The beginning of the study and the end of the study. Method of measurement: PDQL questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina FarahNezhad

Mashhad University of Medical Sciences

m.farahnezhad@yahoo.com+98 912 763 5742

Outcome results

None listed

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