Visual Impairment, Oscillopsia and Multiple Sclerosis
1 other identifier
observational
100
1 country
1
Brief Summary
This study consists of two parts. The first part is a survey to examine vision-specific health-related quality of life in a cohort of patients with multiple sclerosis. We test visual impairment like visual acuity, visual field, colour discrimination, contrast sensitivity, eye movement. The aim of this part is to examine the association between responses to the quality of life scale and objective measures of visual impairment. The second part is an open controlled study, in which we measure motion detection threshold in MS patients with oscillopsia due to pendular nystagmus and in a group of control subjects. The objective of this part is to determine whether patients with pendular nystagmus develop adaptation to oscillopsia using increased threshold of motion detection. We plan to test the effect of visuo-motor rehabilitation on this threshold in patients with oscillopsia due to pendular nystagmus.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2007
CompletedFirst Submitted
Initial submission to the registry
July 6, 2007
CompletedFirst Posted
Study publicly available on registry
July 9, 2007
CompletedSeptember 30, 2010
July 1, 2007
July 6, 2007
September 29, 2010
Conditions
Keywords
Interventions
Eligibility Criteria
Patients with established multiple sclerosis
You may qualify if:
- Age 18 to 90
- Patients with established multiple sclerosis
- Visual impairment recovering from MS
- Understanding rules task
- Patient can stay set a long time
- Patient's agreement
- Membership to the Social Security
- No relapsing since three months
You may not qualify if:
- Brain damage
- Cognitive or behaviour disorder
- Patients with peripheral vestibular, otologic or ophthalmologic pathology antecedent
- Not stabilized disease (other one than MS)
- Patient under guardianship
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Caroline Tilikete
Lyon, 69677, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Caroline Tilikete, MD
Hospices Civils de Lyon
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 6, 2007
First Posted
July 9, 2007
Study Start
April 1, 2007
Last Updated
September 30, 2010
Record last verified: 2007-07