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

Not Applicable
Recruiting
Conditions
Cerebral Neurological Illness
Interventions
Diagnostic Test: Railroad Test
Diagnostic Test: Swamp Test
Diagnostic Test: Presidents Recognition Test
Diagnostic Test: Judgment of Line Orientation
Diagnostic Test: Symbol Span subtest of the Wechsler Memory Scale-IV
Diagnostic Test: Digit Span subtest of the Wechsler Adult Intelligence Scale-I
Diagnostic Test: Reading subtest of the Wide Range Achievement Test
Diagnostic 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
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.
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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.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Non-CNI participantsReading subtest of the Wide Range Achievement TestIdentified 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) participantsJudgment of Line OrientationIdentified 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) participantsSwamp TestIdentified 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) participantsPresidents Recognition TestIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsPresidents Recognition TestIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsJudgment of Line OrientationIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsDigit Span subtest of the Wechsler Adult Intelligence Scale-IIdentified 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) participantsDigit Span subtest of the Wechsler Adult Intelligence Scale-IIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsRailroad TestIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsDot Counting TestIdentified 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) participantsRailroad TestIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsSwamp TestIdentified 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) participantsSymbol Span subtest of the Wechsler Memory Scale-IVIdentified 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) participantsReading subtest of the Wide Range Achievement TestIdentified 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) participantsDot Counting TestIdentified from the department of Rehabilitation, Psychiatry, and Medicine and referred to the research staff via in-person communication, email or staff message
Non-CNI participantsSymbol Span subtest of the Wechsler Memory Scale-IVIdentified 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
NameTimeMethod
Score on Railroad Test1 Day
Score on Swamp Test1 Day
Score on President Recognition Test1 Day
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

New York University School of Medicine

🇺🇸

New York, New York, United States

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