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NCT07520630Not yet recruiting

Neurophysiological Markers for Prediction of Rehabilitation Outcomes After Ischemic Stroke

Neurophysiological Markers for Developing an Integrative Model of Rehabilitation Prognosis in Patients With Ischemic Stroke

Source: ClinicalTrials.gov · Last updated 9 Apr 2026

Brief summary (registry, in English)

The goal of this randomized controlled study is to develop and validate an integrated neurophysiological model for predicting rehabilitation potential in patients with ischemic stroke. The study focuses on identifying objective markers of brain activity associated with motor preparation and recovery. The project includes two stages. First, healthy volunteers will participate in experimental motor and mental tasks to establish reference patterns of brain activity using electroencephalography and transcranial magnetic stimulation. These data will be used to define stable neurophysiological markers of motor network function. In the second stage, patients in the acute and early recovery phases after ischemic stroke will be randomly assigned to receive either active intermittent theta-burst stimulation of the motor cortex or a sham procedure, in addition to standard rehabilitation. Brain activity and clinical motor function will be assessed before and after the intervention. The study aims to determine which neurophysiological measures are sensitive to neuromodulation and are associated with clinical improvement, in order to construct a predictive model of rehabilitation outcome. Participants will \[describe the main tasks participants will be asked to do, interventions they'll be given and use bullets if it is more than 2 items\].

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
5 Mar 2026
Start date
1 May 2026
Primary completion date
31 Mar 2027
Lead sponsor
Moscow Scientific and Practical Center of Medical Rehabilitation, Restorative and Sports Medicine
Diseases
Stroke
NCT number
NCT07520630

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From 1 May 2026 to the primary completion date, 31 Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Epilepsy
  • Severe cardiac arrhythmias
  • Decompensated somatic disease

Other

  • Implanted electronic devices
  • Intracranial aneurysm
  • Pregnancy/lactation

Who the study is looking for

  • First-ever ischemic stroke confirmed by CT/MRI
  • 5 days - 6 months post-stroke
  • Age 40-65
  • MoCA ≥20
  • HADS \<11 for anxiety and depression
  • MRC 2-4 in upper limb
  • Modified Ashworth Scale ≤3
  • Signed informed consent

Criteria the registry did not label

  • Experimental phase:
  • will include healthy volunteers without contradictions to TMS
  • Clinical phase:

Age in the registry: 40 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Moscow Scientific and Practical Center of Medical Rehabilitation, Restorative and Sports Medicine
Coordinator of this site? Confirm its status
MoscowRussiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.