Multiple Sclerosis Clinical Trial

Prevalence of Visual Dysfunction in Neurological Disorders

Summary

The objective is to determine the prevalence of visual dysfunction in People with Parkinson's Disease (PwP). The investigators will administer the: Visual Impairment in Parkinson's Disease Screen and Revised-Self-Report Assessment of Functional Visual Performance. Patients seen at Fixel Institute and their caregivers will be invited to participate. Responses to the 2 questionnaires will help determine prevalence rates of visual dysfunction in PwP compared to those both with and without other neurological conditions.

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Full Description

The purpose of this study is to identify the prevalence of visual dysfunction among Persons with Parkinson's Disease, compared to other neurological conditions and controls without neurological conditions.

Data will be collected anonymously via RedCap. Patients seen at the Fixel Institute that have consented to be contacted regarding research opportunities will be recruited via blast email and advertisement in our Institute's monthly newsletter, the Movement Messenger. The email and newsletter will contain a link for participation in surveys within RedCap so the surveys can be completed anonymously at home. Participation will be completely voluntary and responses will be recorded anonymously. Data will include responses to the following: screening questions, the VIPDQ (Visual Impairment in PD Questionnaire), and the R-SRAFVP (Revised-Self-Report Assessment of Functional Visual Performance).

The investigators will calculate the prevalence of visual impairment (from the VIPDQ) and dysfunction in performance of daily activities (from the R-SRAFVP) for PwP and compare this to the prevalence occurring in other neurological populations as well as the population without any neurological conditions. Other data are collected so the investigators can then evaluate potential confounds or covariates. To ensure statistical methods are accurate, a statistician will be consulted.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Persons with Parkinson's Disease: Confirmed diagnosis of Parkinson's Disease without presence of any other neurological condition.
Persons without Parkinson's Disease (Controls): No previous diagnosis of any neurological condition
Persons with a single other neurological disorder (Neuro Controls): Confirmed diagnosis of other neurological condition (e.g. ALS, multiple sclerosis, essential tremor, ataxia, etc).

Exclusion Criteria:

Children (ages younger than 18 years of age)
Persons with more than one diagnosed neurological condition.

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

10000

Study ID:

NCT04836715

Recruitment Status:

Enrolling by invitation

Sponsor:

University of Florida

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There is 1 Location for this study

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UF Health Rehab - Fixel Institute
Gainesville Florida, 32608, United States
University of Florida
Gainesville Florida, 32608, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

10000

Study ID:

NCT04836715

Recruitment Status:

Enrolling by invitation

Sponsor:


University of Florida

How clear is this clinincal trial information?

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