RECRUITING

Neural Basis of Sensory Learning: Brain Regions

Conditions

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

The purpose of this study is to understand how the sensory and motor areas of the brain work together to keep a person's hand movements accurate (sensorimotor learning). The investigators hope this information may be useful one day to improve rehabilitation techniques in patients with brain lesions.

Official Title

Neural Basis of Sensory Learning: Brain Regions

Quick Facts

Study Start:2021-10-26
Study Completion:2025-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05079516

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 to 45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Potential subjects must be between the ages of 18-45 years old and right-handed. Aging has been shown to affect the morphology of sensory and motor nerves, conduction velocities of nerves, and number of motor neurons in the spinal cord; to avoid these confounding factors we will only examine younger-to middle-aged adults.
  2. * There are differences in cortical function and corticospinal projections such that testing the right arm of a right-handed individual is not necessarily equivalent to testing the left arm of a left-handed individual. To eliminate this confound, we will only test right-handed individuals. All these factors will be determined with the initial screening questions.
  3. * Covid has been found to have neurological effects in some people, but mostly the effects on sensorimotor control and neurophysiology are unknown. So we want to reduce the chances of inadvertently testing subjects who have covid. We will therefore only include individuals who are fully vaccinated (2+ weeks past their final vaccine dose) or have a negative Covid test within 4 days of testing. We will further only include individuals who report being free of Covid symptoms in week preceding testing.
  1. 1. Determined with initial screening questions, pre-enrollment:
  2. 2. Determined on each day of TMS testing:
  3. 3. Determined during the Familiarization session.

Contacts and Locations

Study Contact

Hannah J Block, PhD
CONTACT
8128555390
hjblock@indiana.edu

Principal Investigator

Hannah J Block, PhD
PRINCIPAL_INVESTIGATOR
Indiana University, Bloomington

Study Locations (Sites)

Indiana University Bloomington
Bloomington, Indiana, 47405
United States

Collaborators and Investigators

Sponsor: Indiana University

  • Hannah J Block, PhD, PRINCIPAL_INVESTIGATOR, Indiana University, Bloomington

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 Date2021-10-26
Study Completion Date2025-12

Study Record Updates

Study Start Date2021-10-26
Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

  • Basic Science