Neural Basis of Sensory and Motor Learning: Functional Connections
2 other identifiers
interventional
76
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2022
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
November 4, 2021
CompletedFirst Posted
Study publicly available on registry
November 17, 2021
CompletedStudy Start
First participant enrolled
April 13, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 13, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 13, 2024
CompletedResults Posted
Study results publicly available
January 28, 2026
CompletedJanuary 28, 2026
December 1, 2025
2.2 years
November 4, 2021
December 15, 2025
January 9, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Resting-state PMv-M1 Functional Connectivity (Fisher Z-transformed Correlation)
Brain activity was measured during a 12-minute resting-state functional magnetic resonance imaging (fMRI) scan. Resting-state functional connectivity between the ventral premotor cortex (PMv) and primary motor cortex (M1) was quantified as the Pearson correlation coefficient between the mean blood-oxygen-level-dependent (BOLD) time series extracted from anatomically defined PMv and M1 regions of interest. Correlation coefficients were Fisher z-transformed to improve normality. For each participant, connectivity values were averaged across all scans acquired during the main session. The outcome measure is the mean Fisher z-transformed correlation value (unitless). Numbers range from -1 (opposite activity in the two regions) to 1 (similar activity in the two regions), with 0 implying no relationship between the two regions.
3 scans during the main session (2 hours)
Weighting of Vision vs. Proprioception
Measured by comparing where subjects point on the touchscreen when they are estimating visual vs. proprioceptive targets. A person who relies only on vision would have a weighting value of 100%. A person who relies only on proprioception would have a weighting of 0%. A value of 50% would imply equal reliance on vision and proprioception.
Measured during the main session (2 hours)
Study Arms (1)
Perceptual learning
EXPERIMENTALReaching task in which visual information about target finger position is offset to induce a change in perception of the finger.
Interventions
Reaching task with visual feedback offset from target finger position.
Eligibility Criteria
You may qualify if:
- Ages of 18-45 years old
- Right-handed.
- Free of Covid symptoms in week preceding testing.
You may not qualify if:
- metallic, mechanical, or magnetic implants;
- are claustrophobic, or are unable to remain still for long periods of time;
- use an intra-uterine device (IUD) whos MR compatibility has not been established.
- Women who are pregnant or think they might be pregnant will also be excluded, as effects of fMRI on the unborn are not known.
- 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.
- Potential subjects will be excluded if they have any neurological disorders, or orthopedic or pain conditions in the upper limbs.
- 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.
- 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.
- After giving their consent, participants may be excluded during the study if they are unable to perform the tasks or follow instructions.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Indiana University Bloomington
Bloomington, Indiana, 47405, United States
Results Point of Contact
- Title
- Dr. Hannah Block
- Organization
- Indiana University Bloomington
Study Officials
- PRINCIPAL INVESTIGATOR
Hannah Block
Indiana University, Bloomington
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
November 4, 2021
First Posted
November 17, 2021
Study Start
April 13, 2022
Primary Completion
June 13, 2024
Study Completion
June 13, 2024
Last Updated
January 28, 2026
Results First Posted
January 28, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- ANALYTIC CODE
- Time Frame
- The data will become available when group results are published in peer-reviewed journals
- Access Criteria
- Data will be available on www.osf.io for anyone who wishes to download it. The relevant osf registry will be cited in the peer-reviewed publication so that interested readers can find it.
All IPD that underlie results published in peer-reviewed journals will be shared except individual brain scans.