Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT05478434

Cortico-cortical Stimulation and Robot-assisted Therapy for Upper Limb Recovery After Stroke (CCS&RAT)

Led by I.R.C.C.S. Fondazione Santa Lucia · Updated on 2025-02-20

32

Participants Needed

1

Research Sites

162 weeks

Total Duration

On this page

Sponsors

I

I.R.C.C.S. Fondazione Santa Lucia

Lead Sponsor

U

Università degli studi di Roma Foro Italico

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to tested the effect of combination of a paired associative stimulation of two functional interconnected areas of the cerebral cortex (posterior-parietal cortex and primary motor cortex) with robot-assisted therapy in the recovery of upper limb after stroke.

CONDITIONS

Official Title

Cortico-cortical Stimulation and Robot-assisted Therapy for Upper Limb Recovery After Stroke (CCS&RAT)

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First ever chronic ischemic stroke
  • Hemiparesis due to left or right subcortical or cortical lesion in the territory of the middle cerebral artery
  • Severe or moderate residual upper limb impairment (Fugl-Meyer Assessment motor domain A/D score less than 52)
Not Eligible

You will not qualify if you...

  • History of seizures
  • Severe general impairment or other serious diseases
  • Current treatment with benzodiazepines, baclofen, or antidepressants
  • Intracranial metal implants
  • Cardiac pacemaker
  • Pregnancy
  • Orthopedic conditions preventing upper limb therapy
  • Upper limb pain
  • Cognitive impairment (Mini-Mental State Examination score less than 23)
  • Presence of unilateral spatial neglect

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Santa Lucia Foundation

Rome, Italy, 00179

Actively Recruiting

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Research Team

G

Giacomo Koch, prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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