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Cerebellar Functions in Visuomotor Adaptation

Not Applicable
Conditions
Healthy Participants
Interventions
Other: Focused Ultrasound
Other: Sham
Registration Number
NCT04168086
Lead Sponsor
University of Virginia
Brief Summary

Transcranial focused ultrasound stimulation (tFUS) will be used in this study to functions of the cerebellum in human motor learning. Participants will complete a visuomotor task while receiving stimulation pulses from tFUS. How tFUS stimulation influencing the acquisition and retention of motor memory will be assessed based on group comparison of behavioral measures such as reaching accuracy.

Detailed Description

The purpose of this study is to test functions of the cerebellum in human motor learning. The cerebellum has been thought to play critical roles in human motor control and motor learning. Non-invasive brain stimulation studies with transcranial direct current stimulation (tDCS) and transcranial magnetic stimulation (TMS) provided evidence for the involvement of the cerebellum in human motor learning. However, due to limitations in spatial resolution of tDCS and TMS stimulation, it is still unclear what specific functions the cerebellum may have in motor learning, considering the behavioral and anatomical evidence that the cerebellum also has connections with prefrontal cortex and is associated with cognitive functions. By applying transcranial focused ultrasound stimulation (tFUS), which is a non-invasive brain stimulation technology with great spatial precision, the investigators aim to dissect functions of motor area and non-motor area of the cerebellum in motor learning. Young healthy adults will be recruited and randomly assigned to one of three experimental groups. During learning to adapt to a visual rotation (45 degrees) when reaching for a virtual target, subjects will receive tFUS stimulation over motor area of the cerebellum or non-motor area of the cerebellum depending on the study group. How tFUS stimulation influencing the acquisition and retention of motor memory will be assessed based on group comparison of behavioral measures such as reaching accuracy.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
45
Inclusion Criteria
  • Healthy, adult subjects
  • 18 to 35 years of age
  • Right-handed
  • Provide written informed consent
Exclusion Criteria
  • Presence of a psychiatric or neurologic illness
  • History of loss of consciousness of more than ten minutes in the past year or loss of consciousness in a lifetime that required rehabilitation services
  • Personal or family history of seizure
  • Any history of stroke/transient ischemic attack (TIA) or severe traumatic brain injury
  • Taking any medications that may decrease the threshold for seizure
  • Pregnancy (self-reported)
  • Affirmative answers to one or more questions of the provided attached safety questionnaires. These are not absolute contraindications to this study but the risk/benefit ratio will be carefully balanced by the PI
  • Have any type of metal in the body
  • Failure to follow laboratory or study procedures

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Right Motor Area CerebellumFocused UltrasoundParticipants will receive Focused Ultrasound stimulation to motor area of the right cerebellum prior to completing a motor learning task.
ControlShamParticipants will have the Focused Ultrasound transducer placed on their neck without stimulation as a Sham present prior to completing a motor learning task.
Non-Motor Area CerebellumFocused UltrasoundParticipants will receive Focused Ultrasound stimulation to a non-motor area of the right cerebellum prior to completing a motor learning task.
Primary Outcome Measures
NameTimeMethod
Performance Error on Visuomotor Taskbaseline, immediately after FUS, and 30 minutes after FUS

The visuomotor task has practice, baseline, and experimental trials. Performance on the task will be compared between groups.

Secondary Outcome Measures
NameTimeMethod
Changes in Motor Evoked Potentials (MEP)baseline, immediately after FUS, 10 minutes after FUS, and 20 minutes after FUS

MEPs will be taken at baseline and throughout the task to assess effects ultrasound stimulation has on MEPs.

Trial Locations

Locations (1)

University of Virginia

🇺🇸

Charlottesville, Virginia, United States

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