ImPACT Version 4-Touchscreen: Normative and Reliability Study

ImPACT Applications, Inc.1,437 enrolled

Overview

This research study is designed to establish normative database and reliability of ImPACT for adolescents and adults ages 12 through 80 to expand the use of devices to include touchscreen.

This research study is designed to establish normative database and reliability of ImPACT for adolescents and adults ages 12 through 80 to expand the use of devices to include touchscreen. Enrollment will be 900 participants.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

SCREENING

Masking

NONE

Enrollment

1,437

Conditions

Concussion

Interventions

NormativeDEVICE

ImPACT will be administered at baseline testing

ReliabilityDEVICE

ImPACT will be administered again within 60 days of baseline test

Eligibility

Sex: ALLMin age: 12 YearsMax age: 80 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Age 12-80 2. Primary English speaking or fluent in English Exclusion Criteria: 1. Documentation of a known special education diagnosis other than a 504 designation. 2. History of concussion less than 6 months to the study participation 3. Known physical (e.g., visual impairment not fixable by usual means, such as glasses) or psychological impairment (ADHD, LDD, etc.) that would affect their ability to perform the test.

Locations (1)

ImPACT Applications, Inc.

Coralville, Iowa, United States

Outcomes

Primary Outcomes

Validity

ImPACT Touchscreen performs within normal parameters of ImPACT Online

Time frame: 12 months

Secondary Outcomes

Reliability

Reliability will be established through a test/re-test. ImPACT Touchscreen will be administered at 2 time points to establish results should be stable over time.

Time frame: Baseline test will be administered at enrollment and re-test will be administered within 60 days of baseline test.

Data from ClinicalTrials.gov

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