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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02701842
Other study ID # QPR-16-05
Secondary ID
Status Completed
Phase N/A
First received February 27, 2016
Last updated August 22, 2017
Start date February 2016
Est. completion date September 2016

Study information

Verified date August 2017
Source ImPACT Applications, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The researchers want to find out more about a standalone software application, ImPACT Online and how it relates to other commonly used tests of memory, attention and reaction time. ImPACT Online is a computer-based neurocognitive test for concussion management. The test was designed to help measure the effects of concussion on cognitive processes (for example, memory, attention, brain speed) and visual functioning.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date September 2016
Est. primary completion date June 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 59 Years
Eligibility Inclusion Criteria:

- Age: 12-59

- Primary English speaking or fluent in English.

- No known special education diagnosis excluding a 504 designation.

- Currently not suffering from a concussion or being treated for a concussion.

- No known physical or psychological impairment that would affect their ability to perform the test.

- An average or above average score on the RIST (Reynolds Intellectual Screening Test).

Exclusion Criteria:

- Documentation of a known special education diagnosis other than a 504 designation.

- English is not their primary language nor are they proficient in the English language.

- Currently suffering from a concussion or being treated for a concussion.

- A below average score on the RIST.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ImPACT Online/Paper Pencil Tests

ImPACT Online


Locations

Country Name City State
United States ImPACT Applications Inc. Pittsburgh Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
ImPACT Applications, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Validity is established through correlation studies with well-known measures of memory and processing speed. 12 Months
Primary Reliability will be established through a test/re-test to establish results should be stable over time. 12 Months
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