Neuropsychological Testing Using Mobile Devices

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-31

Study Completion Date

2013-12-31

Brief Summary

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The purpose of this studying is to develop and characterize neuropsychological testing software for evaluating the prefrontal and temporal function of patients. As no software has been used for this purpose, this study will gather pilot data on the baseline performance of patients in a hospital setting that lack any neurological impairment. After creating this baseline, later experiments can be proposed to compare the performance in normal subjects with those who have neurologic injury or disease.

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Detailed Description

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Conditions

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Inpatients With Normal Neurological Function

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Normal patients

for patients with normal score on neurological testing with Folstein Mini-Mental Status Exam will then take the Scenes Task

Group Type OTHER

Neurological testing

Intervention Type BEHAVIORAL

Interventions

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Neurological testing

Intervention Type BEHAVIORAL

Other Intervention Names

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Scenes Task Folstein Mini-Mental Status Exam

Eligibility Criteria

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Inclusion Criteria

* Inpatients \> = 18 years of age
* Patient must be able to provide informed consent

Exclusion Criteria

* Patients with score of \< 26 on Folstein Mini-Mental Status Exam
* Patients with known brain lesions
* Patients with history of stroke, neurologic disease or dementia
* Patients with acute illness or who are in imminent distress

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes