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 type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Virginia Polytechnic Institute and State University Academic / other |
| Locations | 1 site (Blacksburg, Virginia) |
| Status | Recruiting |
| Started | February 29, 2024 |
| Main results expected | July 1, 2027 |
| Study ends | July 1, 2028 |
| Registry record updated | June 17, 2026 |
| Trial ID | NCT06231810 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.
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Remote Ischaemic Conditioning for Fatigue After Stroke 2
Aat least 12 weeks after stroke, adults with post-stroke fatigue will try a simple hand-arm cuff treatment at home to see if it helps reduce fatigue.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.