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Tracking a Tactile Signal Along the Nervous System

Tracking a Tactile Signal Along the Nervous System

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06231810
Enrollment
60
Registered
2024-01-30
Start date
2024-02-29
Completion date
2028-07-01
Last updated
2026-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Tactile Perception

Brief summary

Quantify the flow of a tactile signal from the stimulus at the finger at the peripheral nervous system (PNS), to the central nervous system (CNS), and to cognitive perception at the brain in young adults (Aim 1) and individuals with and without stroke (Aim 2).

Interventions

Tactile stimuli of differing magnitudes will be applied

Sponsors

Virginia Polytechnic Institute and State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Conscious detection threshold30 minutes during the first session of a one session protocolThe magnitude at which a force stimulus applied to the finger can be first consciously detected. Different force levels will be applied, and the participant will indicate which of these forces can be detected. The changes in force applied will be in the units of N.

Secondary

MeasureTime frameDescription
Brain activation60 minutes during the first session of a one session protocolThe magnitude and regions of brain activated in response to differing levels of force stimuli will be captured using fMRI. The % signal change in the brain will be used to define the brain activation in response to each force stimulus level.

Countries

United States

Contacts

CONTACTNetta Gurari, PhD
gurari@vt.edu540-231-3073
PRINCIPAL_INVESTIGATORNetta Gurari, PhD

Virginia Polytechnic Institute and State University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026