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NCT06273475Recruiting

Robot-Assisted Training Versus Standard Training in Ischemic Stroke

The Effect of Robot-Assisted Versus Standard Training on Motor Function Following Subacute Rehabilitation After Ischemic Stroke - a Randomised Controlled Trial Nested in a Prospective Cohort.

Source: ClinicalTrials.gov · Last updated 20 Nov 2025

Brief summary (registry, in English)

The aim of this randomised controlled trial (RCT) nested in a prospective cohort, is to investigate the superior effect of late-phase robot-assisted versus standard training on motor function, physical function, fatigue, and quality of life in a moderately-to-severely impaired chronic stroke population following subacute rehabilitation. The main hypothesis of the study is: Robot-assisted training has a superior effect on motor function (Fugl-Meyer Lower Extremity Assessment; primary outcome), physical function, fatigue, and quality of life in moderately-to-severely impaired chronic stroke-affected individuals in comparison to standard training.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
1 Feb 2024
Start date
1 May 2024
Primary completion date
1 Mar 2026
Lead sponsor
Odense University Hospital
Diseases
Stroke
NCT number
NCT06273475

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 May 2024 to the primary completion date, 1 Mar 2026
  • 2 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.

Criteria the registry did not label

  • Inclusion:
  • Ischemic and haemorrhagic stroke
  • Chronic state (6-24 months post-stroke).
  • Subacute rehabilitation terminated (subacute phase defined as until 6 months post-stroke).
  • Moderately-severely impaired:
    • Modified Rankin Scale Score 3-5.
    • Scandinavian Stroke Scale Leg Motor Function Score 0-4 and/or SSS gait function 0-9.
  • Approved by referring doctor
    • Exclusion:
  • Prior SAH
  • Infarct located in the cerebellum or brain stem
  • Severe fatigue making study completion improbable.
  • Cognitive deficits impeding study participation.
  • Inability to walk independently pre-stroke.
  • Recurrence of cardiovascular/cerebrovascular accidents.
  • Pre-existing neurological diseases or ongoing cancer treatment.
  • Refusing group allocation.
  • Concurrent participation in another clinical trial potentially interacting with the present trial.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
Rigshospitalet and Herlev Gentofte Hospital
Coordinator of this site? Confirm its status
CopenhagenDenmarkNot yet recruiting
Odense University Hospital
Coordinator of this site? Confirm its status
OdenseDenmarkRecruiting

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