RECRUITING

Tracking a Tactile Signal Along the Nervous System

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Conditions

StrokeTactile Perception

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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).

Official Title

Tracking a Tactile Signal Along the Nervous System

Quick Facts

Study Start:2024-02-29
Study Completion:2028-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06231810

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * participants who are neurotypical will be a similar age to the participants with stroke
  2. * participants who are neurotypical will have no musculoskeletal and neurological conditions
  3. * participants with stroke will have a single stroke incident resulting in a unilateral lesion (ischemic and hemorrhagic)
  4. * participants with stroke will be in the chronic phase (\>1 year from stroke onset)
  5. * participants with stroke will have an onset of stroke after the age of 18
  6. * participants with stroke who meet the criteria of having the capacity to provide informed consent, regardless of aphasia
  1. * minors
  2. * pregnant women
  3. * prisoners
  4. * adults not capable of consenting on their own behalf.
  5. * participants with stroke who have used antispastic injections in the past six months
  6. * participants with stroke who have a lesion in the brainstem and/or cerebellum
  7. * participants with stroke who have a stroke arising due to brain surgery
  8. * participants with stroke who have hemineglect

Contacts and Locations

Study Contact

Netta Gurari, PhD
CONTACT
540-231-3073
gurari@vt.edu

Principal Investigator

Netta Gurari, PhD
PRINCIPAL_INVESTIGATOR
Virginia Polytechnic Institute and State University

Study Locations (Sites)

Virginia Tech
Roanoke, Virginia, 24016
United States

Collaborators and Investigators

Sponsor: Virginia Polytechnic Institute and State University

  • Netta Gurari, PhD, PRINCIPAL_INVESTIGATOR, Virginia Polytechnic Institute and State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-29
Study Completion Date2028-07-01

Study Record Updates

Study Start Date2024-02-29
Study Completion Date2028-07-01

Terms related to this study

Additional Relevant MeSH Terms

  • Stroke
  • Tactile Perception