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Study identifier: NCT06070467 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Holistic Mixed Approaches to Capture the Real Life of Children With Rare Eye Diseases

Condition: Eye Diseases · Severe Loss of Vision · Blindness  ·  Sponsor: University Hospital, Strasbourg, France

PhaseN/A
Planned participants154
Who can joinAll sexes, 8 Years to no upper limit
Healthy volunteersYes

About this study

Rare Eye Diseases (RED) are the leading cause of severe visual impairment/ blindness (SVI/B) in children in Europe. This sensory disability with its accompanying psychological distress hugely impacts their lives and their families. Understanding this impact, at a patient centred level, is key in care, in shared decision making, in developing therapies, and in improving social integration and participation about the standard rules of the United Nations (UN) and the European Union (EU) (prevention, non-discrimination, equal opportunities, accessibility, etc.). However, current tools to evaluate vision related (VR) quality of life (QoL) VR-QoL disregard age and cultural differences. There is a lack knowledge on how the disease matters at child's level. Instruments capable of yielding high-quality data, psychometrically robust and comply with regulatory requirements remain to be developed. To fill this gap, SeeMyLife will use multilevel concurrent mixed method research combining quantitative studies and qualitative studies. The quantitative approach is based on (i) cross culturally translated validated VR-QoL questionnaires for children and teenagers (Functional Vision Questionnaire for Children and Young People - FVQ-CYP and Vision-related Quality of Life Questionnaire for Children and Young People - VQoL-CYP) and (ii) on caregiver's questionnaires addressing participation and environment (Participation and Environment Measure - Children and Youth - PEM-CY). To fully capture th…

This description comes directly from the study's public registry record.

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Locations (1)

Centre de Référence pour les Affections Rares en Génétique Ophtalmologique (CARGO), Hôpitaux UniversitairesStrasbourg, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06070467