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Learning in Stroke

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status

Completed

Conditions

Stroke
Sensorimotor Impairment

Treatments

Behavioral: Visuomotor learning task

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05511467
5P20GM109040-10 (U.S. NIH Grant/Contract)
00116626

Details and patient eligibility

About

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.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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 exclusion criteria:

  • Primary intracerebral hematoma
  • subarachnoid hemorrhage
  • bi-hemispheric or cerebellar strokes
  • other concomitant neurological disorders affecting upper extremity motor function
  • documented history of dementia before or after stroke
  • severe aphasia, particularly of receptive nature (NIHSS Language subsection ≥2), affecting their ability to understand the purpose of the study and give informed consent
  • uncontrolled hypertension despite treatment
  • intake of tricyclic anti-depressants or neuroleptic medication.

Trial design

40 participants in 2 patient groups

stroke group
Treatment:
Behavioral: Visuomotor learning task
control group
Treatment:
Behavioral: Visuomotor learning task

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Kelly Krajeck, MHA; Kirstin-Friederike Heise, PhD

Data sourced from clinicaltrials.gov

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