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Neural Basis of Sensory and Motor Learning: Functional Connections

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Basic Science

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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

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 and Motor Learning: Functional Connections

Quick Facts

Study Start:2022-04-13
Study Completion:2024-06-13
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05124301

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. * Ages of 18-45 years old
  2. * Right-handed.
  3. * Free of Covid symptoms in week preceding testing.
  1. * metallic, mechanical, or magnetic implants;
  2. * are claustrophobic, or are unable to remain still for long periods of time;
  3. * use an intra-uterine device (IUD) whos MR compatibility has not been established.
  4. * Women who are pregnant or think they might be pregnant will also be excluded, as effects of fMRI on the unborn are not known.
  5. * People who have a BMI over 30 will be excluded as it may be uncomfortable or impossible to lay in the MRI scanner and reach the button box.
  6. * Potential subjects will be excluded if they have any neurological disorders, or orthopedic or pain conditions in the upper limbs.
  7. * Investigators will also exclude subjects who do not have normal vision, or corrected-to-normal vision with contacts, or the imaging center does not have a pair of MRI compatible glasses that fits their prescription.
  8. * investigators will invite subjects to reschedule if they have any of the common Covid symptoms within the last week and if they haven't been fully vaccinated or obtained a negative Covid test within the past 4 days. If they don't believe they can meet these criteria on another date, they will be excluded.
  9. * After giving their consent, participants may be excluded during the study if they are unable to perform the tasks or follow instructions.

Contacts and Locations

Principal Investigator

Hannah Block
PRINCIPAL_INVESTIGATOR
Indiana University, Bloomington

Study Locations (Sites)

Indiana University Bloomington
Bloomington, Indiana, 47405
United States

Collaborators and Investigators

Sponsor: Indiana University

  • Hannah Block, 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 Date2022-04-13
Study Completion Date2024-06-13

Study Record Updates

Study Start Date2022-04-13
Study Completion Date2024-06-13

Terms related to this study

Additional Relevant MeSH Terms

  • Basic Science