Mobility Protocol Adapted for Advanced Visually Impaired Subjects
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- STATUS
- Recruiting
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- participants needed
- 50
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- sponsor
- Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts
Summary
Retinitis Pigmentosa is characterized by a progressive disappearance of photoreceptors, responsible for a progressive and severe loss of vision.
People Retinitis Pigmentosa therefore encounter a large number of difficulties in daily life, specifically for:
- Visual research
- Visuo-motor coordination in tasks requiring fine motor control
- Visuo-motor coordination in mobility tasks
This study aims to assess the difficulties in the daily life of subjects with Retinitis Pigmentosa at a very advanced stage unsing, quaify of life questionnaires, simplified locomotion tasks in real situation and a posture task.
They are proposing a new test adapted and carried out in real situations, in binocular and monocular vision, making it possible to finely assess locomotion especially for "very low vision" patients.
This test will also ultimately make it possible to better evaluate the effectivements, that is to say to observe and quantify objectively by a score the performance progression obtained for locomotion tasks related to the visual recovery generated by the treatment.
Description
This is monocentric study and the total duration of the study is 48 months. The duration of participation for each research subject is 3 months and maximum 4 visits. This is research involving the human type of non-invasive interventional research, with minimal risks and constraints.
This exploratory study will be conducted on a group of patients with Retinitis Pigmentosa at a very advanced stage.
There will be an inclusion visit including a visual assessment and an ophthalmological consultation. Two experimental visits with tests carried out in a real environment including a locomotion and a posture tasks. An end-of-study visit within a maximum of 1 month following the second experimental visit.
Details
| Condition | Retinitis Pigmentosa, Retinitis Pigmentosa |
|---|---|
| Age | 18years - 75years |
| Treatment | Locomotion task, Posturology task SOT (Sensory Organization Test), The quality of life questionnaire |
| Clinical Study Identifier | NCT04419285 |
| Sponsor | Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts |
| Last Modified on | 19 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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