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Clinical Trials/NCT03502603
NCT03502603
Completed
Not Applicable

Pilot Study of New Computer-based Neuropsychological Tool: Visual Tests, Touch Responses

NYU Langone Health1 site in 1 country137 target enrollmentStarted: May 10, 2019Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
137
Locations
1
Primary Endpoint
Score on Railroad Test

Overview

Brief Summary

This study is aimed at investigating three new tests that will form part of a computerized tool designed to test brain/cognitive functioning. The system will be evaluated along with the tests' usability on samples of healthy controls and neurologically impaired patient participants. These new tests will be assessed with regard to reliability and validity. Reliability will be addressed through investigation of internal consistency of the test items. Validity will be evaluated relative to traditional paper-and-pencil tests and differentiation between patient and healthy participants.Each participant will complete both the computerized and paper and pencil-based tests. The results will be analyzed to see how performances on the two test types compare. The overall aim of this project is to determine if these new computerized tasks are an improvement over standard paper and pencil-based neuropsychological measures.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Individuals without positive cerebral findings on neuroimaging (Non-PCF)
  • Participants can be male or female and between the ages of 21 and 65 years old.
  • Participants will have adequate perceptual and motor capabilities to participate in testing.
  • Neuroimaging-positive cerebral findings (PCF)
  • Patients at NYULMC identified to have significant cerebral findings on neuroimaging.
  • Participants will be male or female and between the ages of 21 and 65 years old.
  • Participants will have adequate perceptual and motor capabilities to participate in testing.

Exclusion Criteria

  • Participants without adequate perceptual and motor capacities preventing them from participation in the testing.
  • Participants with severe dysfunction at the level of dementia that can interfere with informed consent.

Outcomes

Primary Outcomes

Score on Railroad Test

Time Frame: 1 Day

Score on Swamp Test

Time Frame: 1 Day

Score on President Recognition Test

Time Frame: 1 Day

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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