Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06599931

Cerebello-motor Neuromodulation After Stroke. CERSTIM.

Led by Institut National de la Santé Et de la Recherche Médicale, France · Updated on 2026-04-16

45

Participants Needed

2

Research Sites

158 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The CERSTIM study is a physiopatholgical study investigating transcranial alternating current stimulation in stroke patients in the cerebello-motor loop. The design is a cross over design testing two frequencies in the gamma band and one placebo. We will use behavioural data, functional MRI, and Electroencephalography to disentangle the effect of tACS and its frequency. Healthy participants will be also recruited.

CONDITIONS

Official Title

Cerebello-motor Neuromodulation After Stroke. CERSTIM.

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female aged 18 years or older on the day of inclusion
  • Affiliated with a social security system, Universal Health Coverage (CMU), or equivalent
  • For patients: ischemic stroke or intraparenchymal hematoma more than 6 months ago
  • For patients: motor deficit of the upper limb confirmed by ARAT scale with ability to grip and press on a tablet
  • Stroke lesion not affecting the motor cortex in the hand knob area
  • For healthy participants: male or female aged 18 years or older on the day of inclusion
  • For healthy participants: affiliated with a social security system, Universal Health Coverage (CMU), or equivalent
Not Eligible

You will not qualify if you...

  • Pregnant and breastfeeding women
  • Total paralysis of the affected hand
  • Life-threatening conditions or those that could compromise study follow-up
  • Contraindications to MRI and tACS such as ferromagnetic surgical clips, ocular implants, metallic foreign bodies, cochlear implants, brain or cardiac stimulators, or craniotomy scar
  • Participation in another biomedical study focused on motor or overall recovery during the same period or current exclusion period from another biomedical study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

ICM_ Institut du Cerveau et de la Moelle épinière, Hôpital Pitié, 47 Bd de l'Hôpital

Paris, France, 75013

Actively Recruiting

2

ToNIC - Toulouse neuro Imaging center (Inserm)Pavillon Baudot

Toulouse, France, 31300

Not Yet Recruiting

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Research Team

C

Charlotte ROSSO, MD PhD

CONTACT

I

Isabelle LOUBINOUX, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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