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Re-Orchestration of Interregional Oscillatory Activity to Promote Visual Recovery (R4V)

E

Ecole Polytechnique Fédérale de Lausanne

Status

Active, not recruiting

Conditions

Stroke
Parkinson Disease
Visual Impairment

Treatments

Other: Cross-frequency dual-site tACS

Study type

Interventional

Funder types

Other

Identifiers

NCT05220449
2017-01761

Details and patient eligibility

About

This project assesses the effect of bifocal cross-frequency transcranial alternating current stimulation (tACS) combined with visual training to improve visual recovery and orchestrated oscillatory activity in stroke patients suffering from visual field defects.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. the patient can consent for themselves;
  2. age 18+ years old;
  3. at least 7 days since diagnosis "stroke".
  4. Patients should demonstrate a clear deficit in either simple or complex visual perception in portions of their visual field

Exclusion criteria

  1. Diminished capacity to consent;
  2. Pregnancy
  3. Known or suspected non-compliance, drug or alcohol abuse
  4. Inability to follow the procedures of the study, e.g., due to language problems, psychological disorders, dementia, etc. of the participant,
  5. Non-compliance to the instructions of the experimenter or an inappropriate behavior hindering the normal progress of the experiment.
  6. Previous enrolment into the current study
  7. Exclusion criteria of MRI, tACS, TMS
  8. Use of psychoactive medication

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 2 patient groups

Cf-tACS (V1-Alpha_V5-Gamma)
Active Comparator group
Treatment:
Other: Cross-frequency dual-site tACS
Cf-tACS (V1-Gamma_V5-Alpha)
Experimental group
Treatment:
Other: Cross-frequency dual-site tACS

Trial contacts and locations

1

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Central trial contact

Estelle Raffin, PhD; Friedhelm Hummel, Professor

Data sourced from clinicaltrials.gov

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