Examining Lateralized Aspects of Motor Control Using Non-invasive Neural Stimulation
1 other identifier
interventional
60
1 country
1
Brief Summary
Motor adaptation and generalization are believed to occur via the integration of various forms of sensory feedback for a congruent representation of the body's position in space along with estimation of inertial properties of the limb segments for accurate specification of movement. Thus, motor adaptation is often studied within curated environments incorporating a "mis-match" between different sensory systems (i.e. a visual field shift via prism googles or a visuomotor rotation via virtual reality environment) and observing how motor plans change based on this mis-match. However, these adaptations are environment-specific and show little generalization outside of their restricted experimental setup. There remains a need for motor adaptation research that demonstrates motor learning that generalizes to other environments and movement types. This work could then inform physical and occupational therapy neurorehabilitation interventions targeted at addressing motor deficits.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 30, 2023
CompletedFirst Posted
Study publicly available on registry
July 17, 2023
CompletedStudy Start
First participant enrolled
April 3, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 15, 2026
March 13, 2026
March 1, 2026
2.4 years
June 30, 2023
March 12, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Initial direction error, or difference between participant's fingertip direction
Initial direction error, or difference between participant's fingertip direction at the timepoint of peak velocity relative to a linear path to the target. As for time frame, this is a single-visit study. Initial direction error will be compared during baseline reaching and following 20 minutes of non-invasive neural stimulation.
Completion of the study visit, approx 20 minutes
Initial direction error variance
Initial direction error variance across multiple trials.
Completion of the study visit, approx 20 minutes
Secondary Outcomes (4)
Final position error
Completion of the study visit, approx 20 min
Final position error variance across multiple trials.
Completion of the study visit, approx 20 min
Deviation from linearity
Completion of the study visit, approx 20 min
Peak tangential velocity
Completion of the study visit, approx 20 min
Study Arms (3)
Posterior parietal cortex group
EXPERIMENTALPosterior parietal cortex group, which will receive the stimulation to their left posterior parietal cortex
Cerebellum group
EXPERIMENTALCerebellum group, which will receive stimulation to their right cerebellum,
Sham group
SHAM COMPARATORSham group, which will have the electrode cap placed on their head but receive no stimulation
Interventions
By comparing motor adaptation reaching performance between these three groups, the investigators can examine how stimulation to each specific area of the brain modulates different aspects of motor adaptation
Eligibility Criteria
You may qualify if:
- Right-handed as determined by the short-form Edinburgh Handedness Inventory
- Between the ages of 18 and 40
You may not qualify if:
- Mixed- or left-handed as determined by the short-form Edinburgh Handedness Inventory
- Self-reported history of any of the following:
- Seizure and/or diagnosis of epilepsy Fainting spells Concussion with loss of consciousness Ringing in the ears (tinnitus) Cochlear implants Migraines Diagnosed psychological or neurological condition Metal in the scalp
- Any previous adverse reaction to a brain stimulation technique
- Any previous adverse reaction to 3D virtual reality environments (i.e. 'cybersickness')
- Possibility of being currently pregnant (for females only)
- Current open head wound or skin condition of the scalp
- Current implanted device(s) (i.e. cardiac pacemaker)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Virginia Commonwealth University Medical Center
Richmond, Virginia, 23219, United States
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 30, 2023
First Posted
July 17, 2023
Study Start
April 3, 2024
Primary Completion (Estimated)
August 15, 2026
Study Completion (Estimated)
August 15, 2026
Last Updated
March 13, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share