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Combining MyoCI With Memory Reactivation to Improve Motor Recovery After Stroke

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Northwestern University

Status

Enrolling

Conditions

Stroke

Treatments

Other: Targeted Memory Reactivation (TMR)

Study type

Interventional

Funder types

Other

Identifiers

NCT04312269
SP0052149

Details and patient eligibility

About

This study will examine the combination of myoelectric computer interface (MyoCI) training with targeted memory reactivation (TMR) in chronic stroke survivors. The study aims to determine whether this training-plus-sleep combination will generalize to improve arm motor function over an extended training protocol in stroke survivors.

Enrollment

70 estimated patients

Sex

All

Ages

21 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age at enrollment is 21 or older
  • Hemiparesis from first ever stroke affecting arm movement at least 6 months prior to screening
  • Severe to moderate motor impairment (FMA-UE of 7-40)
  • At least some voluntary shoulder and elbow muscle activation

Exclusion criteria

  • Inability to follow instructions of the MyoCI task
  • Visual impairment (such as hemianopia) preventing full view of screen
  • Anesthesia or neglect in the affected arm, or visual hemineglect (score of 2 on the NIH Stroke Scale Extinction and Inattention subtest)
  • Participation in another study on the affected arm within 6 weeks of enrollment or any pharmacological study
  • Inability to understand or follow commands in English due to aphasia or other reason
  • Diffuse or multifocal infarcts in both hemispheres
  • Substantial arm pain preventing participation for 90 minutes a day
  • Spasticity treatment (pharmacological or Botox) within last 3 months
  • Ferromagnetic implants that are MRI incompatible

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 4 patient groups

All phase TMR
Experimental group
Description:
TMR during every stage of sleep
Treatment:
Other: Targeted Memory Reactivation (TMR)
Slow-wave sleep (SWS) only TMR
Experimental group
Description:
TMR during slow-wave sleep only
Treatment:
Other: Targeted Memory Reactivation (TMR)
Reduced frequency TMR
Experimental group
Description:
TMR during only subset of sessions
Treatment:
Other: Targeted Memory Reactivation (TMR)
Sham TMR
Sham Comparator group
Description:
Patients receive no TMR
Treatment:
Other: Targeted Memory Reactivation (TMR)

Trial contacts and locations

1

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Central trial contact

Marc W Slutzky, MD/PhD

Data sourced from clinicaltrials.gov

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