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Search / Trial NCT06471127

Neuroplasticity Biomarkers in Aphasia

Launched by UNIVERSITY OF WISCONSIN, MADISON · Jun 17, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial, called "Neuroplasticity Biomarkers in Aphasia," is studying how the brain can adapt and recover after a stroke, particularly in individuals who experience aphasia. Aphasia is a condition that affects a person's ability to communicate, which can lead to challenges in social interactions, feelings of isolation, and a decrease in overall quality of life. The researchers want to understand the biological markers in the brain that may influence how well someone can recover from aphasia. By identifying these markers, they hope to improve predictions about recovery and find new treatment options to help those affected.

To participate in this trial, individuals need to be between 40 and 90 years old, be right-handed before their stroke, and speak English fluently. They must have had a single stroke affecting a specific part of the brain and currently experience aphasia. Participants will be asked to provide consent and must be medically stable. However, those with major other health issues, significant psychiatric disorders, or certain vision and hearing problems will not be eligible. If you choose to participate, you will be contributing to important research that could lead to better support and treatment for people dealing with aphasia.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Ages 40-90
  • 2. Right-handed (prior to stroke)
  • 3. Proficient English speakers
  • 4. History of a single ischemic stroke in the middle cerebral artery territory that is lateralized to the left or right (Aim 1) cerebral hemisphere.
  • 5. Presence of aphasia (Aims 2-3)
  • 6. Capacity to understand the nature of the study and provide informed consent
  • 7. Acute or subacute stroke at the time of Aim 1 enrollment; Stroke #12 months old (chronic) at the time of Aims 2-3 enrollment
  • 8. Medically stable
  • Exclusion Criteria:
  • 1. History of significant medical or neurological disorder (other than stroke)
  • 2. History of significant or poorly controlled psychiatric disorders
  • 3. Current abuse of alcohol or drugs, prescription or otherwise
  • 4. Clinically significant and uncorrected vision or hearing loss
  • 5. Anything other than standard of care stroke treatment such as Plavix, aspirin (81-300 mg daily), beta-blockers, diabetes medications or choles- terol-lowering agents, thrombolytics (e.g., tPA), anticoagulation agents such as Heparin, Warfarin/Coumadin

About University Of Wisconsin, Madison

The University of Wisconsin-Madison is a leading research institution renowned for its commitment to advancing healthcare through innovative clinical trials. With a strong emphasis on interdisciplinary collaboration, the university leverages its extensive resources, including cutting-edge facilities and a diverse pool of expert researchers, to conduct rigorous studies that address critical health challenges. The institution's focus on translating research findings into practical applications fosters the development of new treatments and interventions, ultimately contributing to improved patient outcomes and public health initiatives. As a sponsor of clinical trials, the University of Wisconsin-Madison is dedicated to upholding the highest ethical standards and ensuring participant safety throughout the research process.

Locations

Madison, Wisconsin, United States

Patients applied

0 patients applied

Trial Officials

Haley Dresang, PhD

Principal Investigator

University of Wisconsin, Madison

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported