Neuropsychological Testing Using Mobile Devices

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01776086

Enrollment

Registered

2013-01-25

Start date

2013-01-31

Completion date

2013-12-31

Last updated

2013-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inpatients With Normal Neurological Function

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.

Interventions

BEHAVIORALNeurological testing

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame	Description
Determination of normal performance curve	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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026