Sign in

NCT04291573Completed

Recovering Arm Function in Chronic Post-stroke Patients Using Combined HD-tDCS and Virtual Reality Therapy

Source: ClinicalTrials.gov · Last updated 12 Jun 2026

Brief summary (registry, in English)

The study aims to determine the added value of combining high-definition transcranial direct current stimulation (HD-tDCS) in a rehabilitation program based on virtual reality therapy (VRT) to potentiate the effects on neuroplasticity and further improve functional recovery of the arm in chronic stroke patients.

Status (registry)
Completed
Study type
Interventional
Enrollment
58 (actual)
First submitted
3 Jan 2020
Start date
1 Feb 2021
Primary completion date
26 Mar 2025
Lead sponsor
University Hospital, Montpellier
Diseases
Stroke
NCT number
NCT04291573

What you commit to

  • Study type: Interventional
  • Participants enrolled: 58
  • From 1 Feb 2021 to the primary completion date, 26 Mar 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.

Other illness

  • Failure to collect written informed consent after a period of reflection
  • History of epilepsy
  • Severe neglect or attention deficit disorder (omission of more than 15 bells in the Bell's test)
  • Severe cognitive impairment (Mini Mental Score \<24)
  • Aphasia with impairment of understanding (Boston Aphasia Quotient \<4/5)

Other

  • Not be affiliated with a French social security scheme or beneficiary of such a scheme
  • Major deficit of the upper extremity (FM-UE \<15)
  • Presence of a pacemaker or a metallic object implanted in the head
  • Pregnant or lactating
  • Under guardianship or curatorship
  • Protected by law

Who the study is looking for

  • Patient aged 18 to 90
  • Patient with more than 3 months of a first cerebrovascular accident whatever the aetiology
  • Patient with paresis of the upper extremity (FM-UE ≥ 15)

Age in the registry: 18 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Montpellier hospital Lapeyronie
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status

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