Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
300 participants
INTERVENTIONAL
2022-04-29
2027-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Use of Sensory Substitution to Improve Arm Control After Stroke
NCT03298243
Effect of Multisensory Stimulation on Upper Extremity Motor Recovery in Stroke Patient: a Preliminary Testing
NCT03094377
Observational Learning in Stroke Patients
NCT00083642
Role of Brain Region Changes in Tactile (Touch) Ability Following Nerve Block
NCT00357058
Sensory Stimulation to Enhance Hand Function Post Stroke
NCT02675764
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
BASIC_SCIENCE
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Conscious awareness: No information
Told nothing about the visuo-proprioceptive mismatch. Hand remains hidden beneath mirror that shows visual display. (control)
Attend to the targets
Participants will not be told anything about the visuo-proprioceptive mismatch. Instead, they will be asked simply to attend to the target positions.
Conscious awareness: Explanatory diagram
Told in advance about the visuo-proprioceptive mismatch, which will be explained with a diagram. Hand remains hidden.
Explanatory diagram
Participant is told there will be a mismatch between their target finger and the visual indicator of target finger position. They will be shown a diagram explaining this.
Conscious awareness: Direct vision of hand
Foamboard under mirror removed, making the mirror see-through and the hand directly visible.
Direct vision
Foamboard under mirror removed, making the mirror see-through and the hand directly visible. Mismatch between target hand and visual indicator will be directly visible.
Movement feedback: No feedback
No movement feedback (control)
No movement feedback
The visual indicator of the target hand will be displaced, but there will be no cursor to indicate the pointing hand's position.
Movement feedback: Target hand
Movement feedback about the target hand.
Movement feedback, target hand
After the participant points at each target, a cursor indicating final pointing position will be displayed briefly. The visual indicator of the target hand will be displaced.
Movement feedback: Pointing hand
Movement feedback about the pointing hand.
Movement feedback, pointing hand
After the participant points at each target, a cursor indicating final pointing position will be displayed briefly. The visual indicator of the target hand will not change, but the cursor indicating pointing hand position will change.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Explanatory diagram
Participant is told there will be a mismatch between their target finger and the visual indicator of target finger position. They will be shown a diagram explaining this.
Direct vision
Foamboard under mirror removed, making the mirror see-through and the hand directly visible. Mismatch between target hand and visual indicator will be directly visible.
Movement feedback, target hand
After the participant points at each target, a cursor indicating final pointing position will be displayed briefly. The visual indicator of the target hand will be displaced.
Movement feedback, pointing hand
After the participant points at each target, a cursor indicating final pointing position will be displayed briefly. The visual indicator of the target hand will not change, but the cursor indicating pointing hand position will change.
No movement feedback
The visual indicator of the target hand will be displaced, but there will be no cursor to indicate the pointing hand's position.
Attend to the targets
Participants will not be told anything about the visuo-proprioceptive mismatch. Instead, they will be asked simply to attend to the target positions.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Right-handed.
* Covid has been found to have neurological effects in some people, but mostly the effects on sensorimotor control and neurophysiology are unknown. So we will only include individuals who report being free of Covid symptoms in week preceding testing.
Exclusion Criteria
* Learning or attention conditions such as ADHD.
* Orthopedic or pain conditions, or a history of seriously injured bones, joints or muscles in either arm.
* Lack of normal or corrected-to-normal vision.
18 Years
45 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institute of Neurological Disorders and Stroke (NINDS)
NIH
Indiana University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hannah Justine Block
Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Hannah J Block
Role: PRINCIPAL_INVESTIGATOR
Indiana University, Bloomington
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hannah Block
Bloomington, Indiana, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
14804
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.