ImPACT Version 4-Touchscreen: Normative and Reliability Study

ImPACT Applications

Status: Active, not recruiting

Conditions: Concussion

Treatments: Device: Normative; Device: Reliability

Study type: Interventional

Funder types: Industry

Identifiers

NCT05551520

QPR-21-20

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 1,437 patients

Sex: All

Ages: 12 to 80 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Screening

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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1,437 participants in 2 patient groups

Normative

Other group

Description:

ImPACT will be administered to participant's for a baseline test.

Treatment:

Device: Normative

Reliability

Other group

Description:

ImPACT will be administered to participant's within 60 days of baseline test.

Treatment:

Device: Reliability