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Treatment of Progressive Multiple Sclerosis-related Cognitive Impairment, Fatigue, and Depression Using Repetitive Transcranial Magnetic Stimulation

Treatment of Progressive Multiple Sclerosis-related Cognitive Impairment, Fatigue, and Depression Using Repetitive Transcranial Magnetic Stimulation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
PACTR
Registry ID
PACTR202403516079512
Enrollment
60
Registered
2024-03-05
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Nervous System Diseases

Interventions

Real repetitive Transcranial Magnetic Stimulation of DLPFC
Real repetitive Transcranial Magnetic Stimulation over SMA
Sham repetitive Transcranial Magnetic Stimulation of DLPFC or of SMA

Sponsors

Science Technology and Innovation Funding Authority
Lead Sponsor
Neurology department Ain Shams University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Definite MS patients according to 2017 revisions of the McDonald criteria. -Progressive types of MS: Patient must fulfill diagnostic criteria of either: Secondary progressive MS (SPMS) or Primary progressive MS (PPMS) -Free of clinical relapses for at least 3 months prior to inclusion. -Free of steroid treatment for at least 6 weeks prior to inclusion. -No change in their medications, whether disease modifying treatment or symptomatic therapy for at least 3 months if applicable. -EDSS score = 6 points and stable over the past 3 months. -A score of <34 on Symbol Digit Modalities Test, a score of = 12 on the Beck Depression Inventory (Beck et al., 1961), a score of = 38 on the Modified Fatigue Impact Scale. -Level of education: at least can read and write. -Written informed consent from the participants

Exclusion criteria

Exclusion criteria: -Conditions that could affect the participants’ level of cognition, fatigue, or depression, including; pregnancy, history of substance use disorder, history of significant neurological disorder other than MS, psychiatric, endocrinological, hepatic, renal, collagen, or other systemic comorbidities that could affect these symptoms. -Contraindication to TMS: history of seizures, skull bone defects, metal fragments in the head, implanted metallic devices such as cardiac pacemakers, cochlear implants, medical pumps…, etc. -Illiterate patients.

Design outcomes

Primary

MeasureTime frame
To investigate the efficacy of high frequency rTMS on cognitive impairment using Symbol Digit Modalities Test, fatigue using Arabic version of Modified Fatigue Impact Scale, and depression using Arabic version of Beck Depression inventory in a sample of Egyptian progressive MS patients.

Secondary

MeasureTime frame
To evaluate the effects of high frequency rTMS on the patients’ MS-related sphincteric dysfunction using the Arabic International Consultation on Incontinence Questionnaire-Short Form Scale, and on the patients’ walking performance using Timed 25-Foot walk test and Functional Ambulation Category.

Countries

Egypt

Contacts

Public ContactAzza Abdelnasser

Professor of Neurology Ain Shams University

azza.abdelnasser@med.asu.edu.eg+201001240246

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026