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ImPACT Version 4-Touchscreen: Normative and Reliability Study

NCT05551520 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1437

Last updated 2023-07-05

No results posted yet for this study

Summary

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.

Conditions

  • Concussion

Interventions

DEVICE

Normative

ImPACT will be administered at baseline testing

DEVICE

Reliability

ImPACT will be administered again within 60 days of baseline test

Sponsors & Collaborators

  • ImPACT Applications, Inc.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-07
Primary Completion
2024-06-01
Completion
2024-10-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05551520 on ClinicalTrials.gov