Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Tracking tactile signals in the nervous system

Official title: Tracking a Tactile Signal Along the Nervous System

Run by Virginia Polytechnic Institute and State University · NCT06231810 · Data updated 2026-11-12

This study is testing how touch signals move from the fingertips to the brain in young adults and stroke survivors to see if there are differences in how they process and perceive these signals.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorVirginia Polytechnic Institute and State University
Academic / other
Locations1 site (Blacksburg, Virginia)
StatusRecruiting
StartedFebruary 29, 2024
Main results expectedJuly 1, 2027
Study endsJuly 1, 2028
Registry record updatedJune 17, 2026
Trial IDNCT06231810 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include right-handed young adults aged 18-23 who are neurotypical, as well as individuals with a history of stroke who meet specific criteria.

Probably not a fit

Patients who are minors, pregnant, or unable to provide informed consent, as well as those with certain neurological conditions or recent antispastic injection treatments, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to quantify how tactile signals travel from the fingertips through the peripheral nervous system to the central nervous system and ultimately to cognitive perception in both young adults and individuals who have experienced a stroke. The research will involve tactile stimulation and will compare neurotypical participants with those who have had a stroke. The study will assess the differences in signal processing and perception between these two groups, focusing on the flow of information through the nervous system.

Why it matters

Potential benefit: If successful, this study could enhance our understanding of tactile perception and improve rehabilitation strategies for stroke patients.

How similar studies have gone: While this approach is innovative, there is limited information on similar studies, indicating that this may be a novel exploration in the field.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

-right-hand dominance for participants who are neurotypical

For Aim 1:

-age range of 18-23

For Aim 2:

* participants who are neurotypical will be a similar age to the participants with stroke
* participants who are neurotypical will have no musculoskeletal and neurological conditions
* participants with stroke will have a single stroke incident resulting in a unilateral lesion (ischemic and hemorrhagic)
* participants with stroke will be in the chronic phase (\>1 year from stroke onset)
* participants with stroke will have an onset of stroke after the age of 18
* participants with stroke who meet the criteria of having the capacity to provide informed consent, regardless of aphasia

Exclusion Criteria:

* minors
* pregnant women
* prisoners
* adults not capable of consenting on their own behalf.

For Aim 2:

* participants with stroke who have used antispastic injections in the past six months
* participants with stroke who have a lesion in the brainstem and/or cerebellum
* participants with stroke who have a stroke arising due to brain surgery
* participants with stroke who have hemineglect

Where it's running

  • Virginia Tech
    Blacksburg, Virginia, United States
    Recruiting

Study contacts

  • Principal investigator: Netta Gurari, PhD — Virginia Polytechnic Institute and State University
  • Study coordinator: Netta Gurari, PhD
  • Email: gurari@vt.edu
  • Phone: 540-231-3073

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.