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NCT07352085Completed

Exoskeleton-assisted Neurorehabilitation

Exoskeleton-assisted Neurorehabilitation: Current Perspectives and Future Directions - A Pilot Study

Source: ClinicalTrials.gov · Last updated 20 Jan 2026

Brief summary (registry, in English)

* Objective assesment of the feasibility of integrating the Ekso Bionics - Ekso NR device into outpatient care * Objective assesment of quality of life, functionality and clinical symptomps of patients with stroke, cerebellar ataxia, spinal cord injury, and spastic paraparesis * Comparison of measured data and follow-up of changes in relation to themselves and each other * Analyzing the effects of the exoskeleton among the patients * Assessing the safety, possible side effects and tolerability of the EksoNR

Status (registry)
Completed
Study type
Interventional
Enrollment
5 (actual)
First submitted
10 Jan 2026
Start date
1 Jun 2024
Primary completion date
28 Feb 2025
Lead sponsor
Somogy Megyei Kaposi Mór Teaching Hospital
Diseases
Stroke
NCT number
NCT07352085

What you commit to

  • Study type: Interventional
  • Participants enrolled: 5
  • From 1 Jun 2024 to the primary completion date, 28 Feb 2025
  • 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.

Prior treatment

  • irregular medication use
  • drug use
  • current participation in individual or group exercise program outside of standard physical therapy

Other illness

  • severe heart disease
  • seizure disorder
  • untreated diabetes
  • severe visual or hearing impairment
  • smoking after diagnosis of stroke

Other

  • height below 150 cm or above 190 cm
  • body weight exceeded 100 kg
  • multiple strokes in medical history
  • systolic blood pressure less than 120 or higher than 160 mmHg
  • orthostatic hypotension
  • arotid artery stenosis
  • hemophilia
  • traumatic brain injury
  • abnormal electroencephalography
  • abnormal blood panel
  • use of sedatives
  • severe aphasia (Western Aphasia Battery ≤ 25)
  • severe sensory dysfunction
  • severe orthopedic problems
  • alcoholism
  • unable to walk at least 10 m with or without assistance in 6 minutes
  • BBS score ≤ 32
  • BI score ≤ 70

Who the study is looking for

  • confirmed diagnosis of spinal cord injury (at or below the C4 level)
  • having cerebellar ataxia diagnosis
  • confirmed spastic paraparesis
  • ischemic stroke

Age in the registry: 18 years to 80 years · Sex: All · Does not accept 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
Somogy County Kaposi Mór Teaching Hospital
Coordinator of this site? Confirm its status
KaposvárHungaryUnknown status

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