General information
  • Disease category Other (BASEC)
  • Recruitment status recruitment not started yet (BASEC/ICTRP)
  • Trial sites
    Bern, Geneva
    (BASEC)
  • Contact Adrian Guggisberg adrian.guggisberg@hug.ch (BASEC)
  • Data Source(s) BASEC: Import from 19.01.2026 ICTRP: N/A
  • Last update 19.01.2026 09:00
HumRes67357 | SNCTP000006611 | BASEC2025-00765

Vision Training with Neurofeedback

  • Disease category Other (BASEC)
  • Recruitment status recruitment not started yet (BASEC/ICTRP)
  • Trial sites
    Bern, Geneva
    (BASEC)
  • Contact Adrian Guggisberg adrian.guggisberg@hug.ch (BASEC)
  • Data Source(s) BASEC: Import from 19.01.2026 ICTRP: N/A
  • Last update 19.01.2026 09:00

Summary description of the study

Visual field deficits are a common consequence of acquired brain injuries and affect people of all ages. These visual problems make daily life more challenging – for example, when reading, driving, or moving safely. However, there is currently no effective therapy to improve visual field deficits. Previous training methods have focused on maximizing brain activity during a task. However, new findings show that the best performance is achieved when the brain is already in a state of high communication before the task. Our research shows that people can learn to enhance communication between brain regions through neurofeedback. Studies have shown that neurofeedback can help people after a stroke: it improves the collaboration of brain areas important for movement – and can thus help to increase mobility. Building on these results, this study investigates whether EEG neurofeedback can support the visual center in the brain to improve vision in patients with chronic visual field deficits. The main goal of the study is to evaluate the effectiveness of neurofeedback in improving visual field deficits. More specifically, we examine the development of visual ability (expansion of the visual field, contrast sensitivity). The neurofeedback method has already been studied with healthy participants at Inselspital Bern, but it is not yet approved in Switzerland for the treatment of visual field deficits. This study aims to show whether neurofeedback can improve visual ability in patients with chronic visual field deficits.

(BASEC)

Intervention under investigation

This study investigates how EEG neurofeedback works. Electrodes on the scalp measure brain activity, and participants receive immediate feedback – in the form of sounds. The sounds indicate how well they succeed in activating certain areas of the brain. The goal is to improve collaboration between the visual areas of the brain to promote vision. Additionally, all participants undergo a magnetic resonance imaging (MRI) scan. This helps us to fine-tune the neurofeedback to the brain more accurately.

(BASEC)

Disease under investigation

Visual field deficits after stroke

(BASEC)

Criteria for participation in trial
- Chronic and stable visual field deficits - 12 months or more after a stroke - Age between 50 and 70 years - Ability to provide informed consent (BASEC)

Exclusion criteria
- Inability to concentrate during longer therapy sessions - Eye diseases affecting the visual field - Non-MRI-compatible metal in the body - New stroke during the study period - Presence of a spatial processing disorder (neglect) (BASEC)

Trial sites

Bern, Geneva

(BASEC)

not available

Sponsor

Adrian Guggisberg Service de Neurorééducation, Hôpitaux Universitaires de Genève

(BASEC)

Contact

Contact Person Switzerland

Adrian Guggisberg

+41 (0) 22 372 37 00

adrian.guggisberg@hug.ch

Service de Neurorééducation, Hôpitaux Universitaires de Genève

(BASEC)

Scientific Information

not available

Name of the authorising ethics committee (for multicentre studies, only the lead committee)

Ethics Committee Geneva

(BASEC)

Date of authorisation

30.09.2025

(BASEC)


ICTRP Trial ID
not available

Official title (approved by ethics committee)
Neurofeedback-based Visual Restoration Therapy (BASEC)

Academic title
not available

Public title
not available

Disease under investigation
not available

Intervention under investigation
not available

Type of trial
not available

Trial design
not available

Inclusion/Exclusion criteria
not available

not available

Primary and secondary end points
not available

not available

Registration date
not available

Incorporation of the first participant
not available

Secondary sponsors
not available

Additional contacts
not available

Secondary trial IDs
not available

Results-Individual Participant Data (IPD)
not available

Further information on the trial
not available

Results of the trial

Results summary

not available

Link to the results in the primary register

not available