Development of a Neurocognitive Screening Test
Stopped early · Not applicable
Conditions studied: Brain Concussion, Mild Cognitive Impairment
In brief
This research study will evaluate a standalone software application and is designed to standardize and validate new neurocognitive screening testing for children aged 6 through 11, and adolescents and adults ages 12 through 75. The purpose of this study is to evaluate recently developed computerized tasks sensitive to changes in neurocognitive performance after a concussion. These tests were designed to help measure the effects of concussion on cognitive processes (e.g., memory, attention, brain speed) and visual functioning.
Key facts
- Study ID
- NCT02597504
- Run by
- ImPACT Applications, Inc.
- People needed
- 1600
- Starts
- 2015-10-01
- Expected to finish
- 2019-10-01
- Last updated by the study team
- 2023-09-29
Who can join
Age: 6 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age: 12-75 (Adult version), 6-11 (pediatric version)
- 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.
You may not qualify if…
- 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.*
- Any known physical or psychological impairment that would affect their ability to perform the test.
- Note: Unless specifically required by the particular study (i.e., a discriminant validity study differentiating concussed versus non-concussed individuals).
Where it is running
- FastMed Urgent Care — Scottsdale, Arizona, United States
- University of Arkansas — Fayetteville, Arkansas, United States
- Head First — Crofton, Maryland, United States
- Jim Gyurke — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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