Stroke Trial, Recruiting NCT05303649 Sponsor: Institute of Psychiatry and Neurology, Warsaw Condition: Stroke
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Stroke Trial, Recruiting

NCT05303649
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have had their first-ever stroke caused by a blocked artery on the left side of the brain, confirmed by an MRI scan
  • People who are at least 3 months past the date their stroke occurred
  • People who have a type of language difficulty called non-fluent aphasia, confirmed by a specific language test, with communication challenges ranging from mild to significant, particular trouble finding and naming words, and relatively preserved understanding of everyday speech
  • People who are native Polish speakers
  • People who were right-handed before their stroke
  • People who are willing and able to sign a consent form to take part in the study

Who may not be able to join:

  • People who have a psychiatric or neurological condition in addition to their stroke, such as dementia, depression, or alcohol dependence
  • People who have been diagnosed with epilepsy, have shown epilepsy-related changes on a brainwave (EEG) test, or who frequently lose consciousness in ways that might suggest seizures
  • People who have previously had any surgical procedure involving the head or brain
  • People for whom an MRI scan at 1.5 Tesla strength is not safe — for example, those with certain metal devices in their body such as a heart defibrillator or deep brain stimulation device, or those with claustrophobia
  • People who regularly take medications that could affect brain activity or the brain's ability to adapt, such as anti-epileptic drugs, antipsychotics, antidepressants, benzodiazepines, or dopamine-related medications
  • People with significant thinking or memory difficulties that would limit their ability to take part in assessments and therapy sessions
  • People with serious vision problems that would make it difficult to see tasks displayed on a computer screen during therapy
  • People who experience a new neurological event (such as another stroke) or a serious illness (such as COVID-19) during the therapy period that requires treatment to be stopped

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Katarzyna E Polanowska, PhD, Institute of Psychiatry and Neurology, Warsaw, Poland

Phone: +48224582870

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Institute of Psychiatry and Neurology, Warsaw
Registry
ClinicalTrials.gov
Start date
2 September 2022
Est. completion
1 December 2027

Where this trial is recruiting

🇵🇱 Poland

Primary endpoints

Change from pre-treatment assessment in the performance on a picture naming task; Change from pre-treatment in the performance on the picture naming task at 3 months post-therapy (follow up assessment); Change from post-treatment in the performance on the picture naming task at 3 months post-therapy; Change from pre-treatment assessment in the performance on a scene description task of three visually presented scenes; Change from pre-treatment in the scene description task at 3 months post-therapy; Change from post-treatment in the scene description task at 3 months post-therapy; Change from p...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov