Clinical trial · Interventional
Effectiveness of a Visual Telerehabilitation Program on Visual Perception in Children, Adolescents and Young Adults With Hemianopsia Consecutive to a Brain Tumour
NCT07558395CI-TRIAL-00109950REVIIH-BTnot yet recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 17, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260917-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hemianopsia | — | UNRESOLVED | — |
| Pediatric Brain Tumor | Childhood Brain Neoplasm | ALIAS | 0.90 |
| Virtual Reality | — | UNRESOLVED | — |
| Visual Rehabilitation | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| standard of care | Other | — | UNRESOLVED |
| Visual Stimulation | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- OTHER
- label
- Control
- description
- Standard of care for the first 8 weeks then visual stimulation for the following 8 weeks
- interventionNames
- Device: Visual Stimulation
- Other: standard of care
- type
- OTHER
- label
- Intervention
- description
- Visual stimulation for the first 8 weeks then standard of care for the following 8 weeks
- interventionNames
- Device: Visual Stimulation
- Other: standard of care
Primary outcomes (1)
- measure
- Visual field perimetry measured using the Esterman binocular field test
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 10 Years
- Maximum age
- 40 Years
Show eligibility criteria text
Inclusion Criteria: * 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 Exclusion Criteria: * Age\< 10 years old of \> 40 years old * Ocular disease * Inability to perform during testing or training * 3 consecutive VRISE scores \< 25 at inclusion * History of vertigo * Prior vision rehabilitation interventions * Recreational or medicinal consumption of psychoactive drugs * Persons under court protection * Interpupillary distance \< 54mm
References
Publications (0)
Data not yet available
No reference posted for this study.