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NCT03574623Completed

Therapies for Recovery of Hand Function After Stroke

Contralaterally Controlled FES Versus Cyclic NMES for Hand Function After Stroke

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

After a stroke, it is very common to lose the ability to open the affected hand. The purpose of this study is to compare the effects of three different therapies on recovery of hand function after stroke and determine if any one is better than the other.

Status (registry)
Completed
Study type
Interventional
Enrollment
132 (actual)
First submitted
20 Jun 2018
Start date
15 Feb 2019
Primary completion date
16 Oct 2024
Lead sponsor
MetroHealth Medical Center
Diseases
Stroke
NCT number
NCT03574623

What you commit to

  • Study type: Interventional
  • Participants enrolled: 132
  • From 15 Feb 2019 to the primary completion date, 16 Oct 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • concurrent enrollment in another investigational study

Other illness

  • co-existing neurologic diagnosis of peripheral nerve injury, Parkinson's disease, spinal cord injury, traumatic brain injury, or multiple sclerosis
  • uncontrolled seizure disorder
  • brainstem stroke
  • history of potentially fatal cardiac arrhythmias with hemodynamic instability
  • diagnosis (apart from stroke) that substantially affects paretic arm and hand function

Other

  • uncompensated hemineglect
  • severe shoulder or hand pain
  • insensate forearm or hand
  • implanted electronic systems (e.g. pacemaker)
  • botulinum toxin injections to any upper extremity muscle within 3 months of enrolling
  • pregnant women due to unknown risks of surface NMES during pregnancy
  • lack of functional passive range of motion of the wrist or fingers of affected side
  • deficits in communication that interfere with reasonable study participation
  • lacking sufficient visual acuity to see the stimulator's display

Who the study is looking for

  • 6 to 24 months since a first clinical cortical or subcortical, hemorrhagic or nonhemorrhagic stroke
  • unilateral upper limb hemiparesis with finger extensor strength of grade no more than 4 out of 5 on the Medical Research Council (MRC) scale
  • score of at least 1 and no more than 11 out of 14 on the hand section of the upper extremity Fugl-Meyer Assessment
  • adequate active movement of the shoulder and elbow to position the hand in the workspace for table-top task practice (necessary for the lab task practice sessions)
  • able to follow 3-stage commands
  • able to recall at least 2 of a list of 3 items after 30 minutes
  • skin intact on the hemiparetic arm
  • surface stimulation of the paretic finger and thumb extensors produces functional hand opening without pain (this will exclude those who have too much flexor spasticity)
  • able to hear and respond to cues from stimulator
  • not receiving occupational therapy (no concomitant OT)
  • full voluntary opening/closing of the contralateral (less affected) hand
  • demonstrates ability to follow instructions for operating the stimulator or have a caregiver who will assist them

Age in the registry: 21 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University and Atlanta VA
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Johns Hopkins University
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
MetroHealth Rehabilitation Institute
Coordinator of this site? Confirm its status
ClevelandUnited StatesUnknown status
Kessler Foundation
Coordinator of this site? Confirm its status
West OrangeUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.