Effectiveness of a Visual Telerehabilitation Program on Visual Perception in Children, Adolescent… (NCT07558395) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effectiveness of a Visual Telerehabilitation Program on Visual Perception in Children, Adolescents and Young Adults With Hemianopsia Consecutive to a Brain Tumour
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.
Who can participate
Age range
10 Years – 40 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Visual field perimetry measured using the Esterman binocular field test
Timeframe: From enrollment to the end of follow up period at 6 months
Trial details
NCT IDNCT07558395
SponsorInstitut National de la Santé Et de la Recherche Médicale, France