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Clinical Trials/NCT01776086
NCT01776086WithdrawnNot Applicable

Neuropsychological Testing Using Mobile Devices

Englewood Hospital and Medical Center2 sites in 1 countryStarted: January 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
2
Primary Endpoint
Determination of "normal performance" curve

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

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

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

Outcomes

Primary Outcomes

Determination of "normal performance" curve

Time Frame: 1 year

The purpose of this study is to generate a curve of "normal performance" on the neurological test for hospitalized patients of different ages

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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