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Learning in Stroke

Neural Circuitries of Motor Learning as a Target to Modulate Sensorimotor Recovery After Stroke

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05511467
Enrollment
40
Registered
2022-08-23
Start date
2022-09-01
Completion date
2025-09-30
Last updated
2025-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sensorimotor Impairment, Stroke

Keywords

procedural learning, maladaptive plasticity

Brief summary

After a stroke, plasticity occurs in the brain from microscopic to network level with positive but also negative consequences for functional recovery. Why post-stroke plasticity takes a beneficial or a maladaptive direction is still incompletely understood. Because the biological mechanisms underlying sensorimotor learning parallel those observed during recovery, learning mechanisms could be potential modifiers of post-stroke neuroplasticity and have a discrete mal-/adaptive impact on the recovery of sensorimotor function. This project seeks to further the understanding of the link between brain circuits that control the integration of new information during procedural learning in the injured brain and those circuits that are involved in adaptive plastic changes during recovery of sensorimotor function post-stroke. The project's methodological approach will allow the characterization of procedural learning-related neural network dynamics based on functional magnetic resonance imaging (MRI) in human volunteers with and without neurologically impairment post-stroke. Through multivariate integration of behavioral and biological descriptors of sensorimotor recovery, the project will investigate the association between motor learning-related network dynamics and descriptors of recovery.

Interventions

BEHAVIORALVisuomotor learning task

Participants undergo functional magnetic resonance imaging during the performance of the visuomotor learning task. The visuomotor learning task involves holding a device in the hand that measures the strength of the grip when squeezing the 'gripper'.

Sponsors

National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH
Medical University of South Carolina
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

For all participants: * adult volunteers (age ≥18 years) * right-hand dominance as defined by the Edinburgh Handedness Inventory Stroke-specific inclusion criteria: * ischemic or hemorrhagic lesion * subcortical or cortical tissue involvement * chronic phase (\>6 months) after their index lesion * voluntary whole-hand grip force (MRC, Medical Research Council scale for muscle force ≥2) * repeated release (standardized as a reduction of 50% of maximum voluntary contraction measured with a dynamometer)

Exclusion criteria

For all participants: * Presence of any MRI risk factors * substance use disorder * psychotic disorders Stroke-group specific

Design outcomes

Primary

MeasureTime frameDescription
Learning Rate as Indexed by Change in the Precision of Visuomotor Grip Force Adjustment (i.e., Reduction of Precision Error in Force Adjustment)Pre Learning Session and Post Learning Session (approximately 90 minutes)Isometric whole-hand grip force is captured continuously with grip-force transducers (at 1000Hz) and adjusted relative to the individual maximum voluntary contraction. Precision of force adjustment is based on the recorded muscle force monitored during task performance and defined as the actual force exerted by the participant relative to the target force (measurement unit: precision in %), with positive values indicating over- and negative values indicating undershoot. Learning rate from before to after learning will be defined as the difference in precision between before as compared to after one single learning session. Precision error was calculated as the percentage deviation of the actual grip force from the target force, averaged across trials before and after the learning task. A reduction in force error indexes a behavioral advantage of force adjustment over time and is thus interpreted as learning.
Change in Blood-oxygen-level-dependent (BOLD) Signal Derived Multi-voxel Brain ActivationPre Learning Session and Post Learning Session (approximately 90 minutes)Learning-related BOLD-signal-derived brain activation relative to motor performance.

Countries

United States

Participant flow

Recruitment details

Recruitment period 09/01/2022 - 03/30/2024

Participants by arm

ArmCount
stroke group
Visuomotor learning task: Participants undergo functional magnetic resonance imaging during the performance of the visuomotor learning task. The visuomotor learning task involves holding a device in the hand that measures the strength of the grip when squeezing the 'gripper'.
25
control group
Visuomotor learning task: Participants undergo functional magnetic resonance imaging during the performance of the visuomotor learning task. The visuomotor learning task involves holding a device in the hand that measures the strength of the grip when squeezing the 'gripper'.
15
Total40

Baseline characteristics

Characteristiccontrol groupTotalstroke group
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
7 Participants16 Participants9 Participants
Age, Categorical
Between 18 and 65 years
8 Participants24 Participants16 Participants
Age, Continuous60 years59.5 years59 years
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
13 Participants26 Participants13 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
2 Participants14 Participants12 Participants
Region of Enrollment
United States
15 Participants40 Participants25 Participants
Sex: Female, Male
Female
8 Participants19 Participants11 Participants
Sex: Female, Male
Male
7 Participants21 Participants14 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 250 / 15
other
Total, other adverse events
0 / 251 / 15
serious
Total, serious adverse events
0 / 250 / 15

Outcome results

Primary

Change in Blood-oxygen-level-dependent (BOLD) Signal Derived Multi-voxel Brain Activation

Learning-related BOLD-signal-derived brain activation relative to motor performance.

Time frame: Pre Learning Session and Post Learning Session (approximately 90 minutes)

Population: One stroke group participant was excluded because of poor data quality (excessive movement inside the MRI). One control group participant excluded due to incidental findings.

ArmMeasureValue (MEAN)
stroke groupChange in Blood-oxygen-level-dependent (BOLD) Signal Derived Multi-voxel Brain Activation2.6 percentage of BOLD signal change
control groupChange in Blood-oxygen-level-dependent (BOLD) Signal Derived Multi-voxel Brain Activation3.25 percentage of BOLD signal change
Primary

Learning Rate as Indexed by Change in the Precision of Visuomotor Grip Force Adjustment (i.e., Reduction of Precision Error in Force Adjustment)

Isometric whole-hand grip force is captured continuously with grip-force transducers (at 1000Hz) and adjusted relative to the individual maximum voluntary contraction. Precision of force adjustment is based on the recorded muscle force monitored during task performance and defined as the actual force exerted by the participant relative to the target force (measurement unit: precision in %), with positive values indicating over- and negative values indicating undershoot. Learning rate from before to after learning will be defined as the difference in precision between before as compared to after one single learning session. Precision error was calculated as the percentage deviation of the actual grip force from the target force, averaged across trials before and after the learning task. A reduction in force error indexes a behavioral advantage of force adjustment over time and is thus interpreted as learning.

Time frame: Pre Learning Session and Post Learning Session (approximately 90 minutes)

Population: One stroke group participant was excluded because of poor data quality (excessive movement inside the MRI). One control group participant excluded due to incidental findings.

ArmMeasureValue (MEDIAN)
stroke groupLearning Rate as Indexed by Change in the Precision of Visuomotor Grip Force Adjustment (i.e., Reduction of Precision Error in Force Adjustment)-1.48 Percentage deviation from target force
control groupLearning Rate as Indexed by Change in the Precision of Visuomotor Grip Force Adjustment (i.e., Reduction of Precision Error in Force Adjustment)0.303 Percentage deviation from target force

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026