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NCT05996198Completed

Exoskeletal Support in Stroke

A Pilot Proof of Concept, Single Site Study to Assess the Effect of Exoskeletal Support on Motor Control Strategies in Individuals With Stroke

Source: ClinicalTrials.gov · Last updated 1 Apr 2025

Brief summary (registry, in English)

This interventional study will measure motor performance, including 3D movement analysis and muscle activity, in response to exoskeleton assistance. The cohort design will compare stroke patients to healthy controls. Data collection will be conducted in a single, 2-hour session. Investigators will also access stroke patients' brain MRIs that were obtained as standard of care during acute admission for stroke.

Status (registry)
Completed
Study type
Interventional
Enrollment
19 (actual)
First submitted
9 Aug 2023
Start date
3 Jan 2024
Primary completion date
29 Apr 2024
Lead sponsor
NYU Langone Health
Diseases
Stroke
NCT number
NCT05996198

What you commit to

  • Study type: Interventional
  • Participants enrolled: 19
  • From 3 Jan 2024 to the primary completion date, 29 Apr 2024
  • 1 site 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.

Other illness

  • have any conditions that limit their capability of using a Head Mounted Display (HMD) for a VR environment or cooperate with the protocol.
  • Have neurological injuries other than stroke.

Other

  • All participants
  • have any orthopedic injuries to the upper extremities.
  • Have excessive pain in any joint of either arm that could limit the ability to cooperate with the protocols.
  • Visuospatial neglect
  • Apraxia
  • Global inattention
  • Legal blindness

Who the study is looking for

  • Healthy controls:
  • Having obtained the age of 18 years
  • Neurologically healthy (i.e., no history of: traumatic brain injury, peripheral neuropathy, seizures, etc.)
  • Strongly right-handed according to at least 80% score on the Edinburgh Handedness Inventory (Oldfield, 1971; Veale, 2013). The use of right-handed participants is a common feature in this field of study. This is due to the slight differences in arm control between left- and right-handed individuals (Sainburg \& Kalakanis, 2000).
  • Ability to give informed consent
    • Survivors of stroke:
  • Having obtained the age of 18 years
  • have a diagnosis of stroke more than six months prior to entry into the study;
  • have the ability to reach, unsupported, to approximately 70% of arm length
  • ability to give informed consent

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
NYU Langone Health (222 East 41st Street)
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

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