Pilot Study of New Computer-based Neuropsychological Tool: Visual Tests, Touch Responses
- Conditions
- Cerebral Neurological Illness
- Interventions
- Diagnostic Test: Railroad TestDiagnostic Test: Swamp TestDiagnostic Test: Presidents Recognition TestDiagnostic Test: Judgment of Line OrientationDiagnostic Test: Symbol Span subtest of the Wechsler Memory Scale-IVDiagnostic Test: Digit Span subtest of the Wechsler Adult Intelligence Scale-IDiagnostic Test: Reading subtest of the Wide Range Achievement TestDiagnostic Test: Dot Counting Test
- Registration Number
- NCT03502603
- Lead Sponsor
- NYU Langone Health
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
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.
- 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Non-CNI participants Reading subtest of the Wide Range Achievement Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Judgment of Line Orientation Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Swamp Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Presidents Recognition Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Presidents Recognition Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Judgment of Line Orientation Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Digit Span subtest of the Wechsler Adult Intelligence Scale-I Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Digit Span subtest of the Wechsler Adult Intelligence Scale-I Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Railroad Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Dot Counting Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Railroad Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Swamp Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Symbol Span subtest of the Wechsler Memory Scale-IV Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Reading subtest of the Wide Range Achievement Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Cerebral neurological illness (CNI) participants Dot Counting Test Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message Non-CNI participants Symbol Span subtest of the Wechsler Memory Scale-IV Identified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
- Primary Outcome Measures
Name Time Method Score on Railroad Test 1 Day Score on Swamp Test 1 Day Score on President Recognition Test 1 Day
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
New York University School of Medicine
🇺🇸New York, New York, United States