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NCT07558395Not yet recruiting

Effectiveness of a Visual Telerehabilitation Program on Visual Perception in Children, Adolescents and Young Adults With Hemianopsia Consecutive to a Brain Tumour

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

Evaluate the efficiency of audiovisual stimulation in virtual reality for improving the visual perception of children, adolescents, and young adults with hemianopia resulting from pediatric brain tumors. These individuals can lose up to 50% of their visual field, significantly impacting their independence, mobility, and daily lives.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
25 Nov 2025
Start date
Dec 2026
Primary completion date
Dec 2026
Lead sponsor
Institut National de la Santé Et de la Recherche Médicale, France
NCT number
NCT07558395

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From Dec 2026 to the primary completion date, Dec 2026
  • 8 sites in 7 countries
  • 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.

Prior treatment

  • Prior vision rehabilitation interventions
  • Recreational or medicinal consumption of psychoactive drugs

Other illness

  • Ocular disease
  • History of vertigo

Age

  • Age\< 10 years old of \> 40 years old

Other

  • Inability to perform during testing or training
  • 3 consecutive VRISE scores \< 25 at inclusion
  • Persons under court protection
  • Interpupillary distance \< 54mm

Who the study is looking for

  • Male and Female
  • 10 - 40 years old
  • Diagnosed hemianopsia (\>12 months)
  • History of diagnosis brain tumour
  • Being stable for the tumour for \> 6 months (either on therapy or not)
  • Visual acuity ≤ 0.7 LogMAR
  • Ability to follow the visual and auditory stimuli and training instructions
  • Home WiFi access
  • Ability to attend all on site visits
  • Affiliation to the Social Security or beneficiary of such social protection

Age in the registry: 10 years to 40 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (8)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Paediatric and adolescents medicine, Medical University
Coordinator of this site? Confirm its status
ViennaAustriaUnknown status
Paediatrics and Adolescents Medicine, University Hospital
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status
Paediatric Oncology, San Joan de Deu
Coordinator of this site? Confirm its status
BarcelonaSpainUnknown status
Hôpital de Hautepierre
Coordinator of this site? Confirm its status
StrasbourgFranceUnknown status
Great Ormond Street Hospital for Children
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status
Institute of Tumour, department of haematology and Oncohaematology paediatric
Coordinator of this site? Confirm its status
MilanItalyUnknown status
Paediatric Haematology, University Hospital
Coordinator of this site? Confirm its status
PadovaItalyUnknown status
Princess Maxima Centre for Paediatric Oncology
Coordinator of this site? Confirm its status
UtrechtNetherlandsUnknown status

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