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临床试验/NCT05551520
NCT05551520进行中(未招募)不适用

ImPACT Version 4-Touchscreen: Normative and Reliability Study

ImPACT Applications, Inc.1 个研究点 分布在 1 个国家目标入组 1,437 人开始时间: 2022年2月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,437
试验地点
1
主要终点
Validity

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

入排标准

年龄范围
12 Years 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Primary English speaking or fluent in English

排除标准

  • •Documentation of a known special education diagnosis other than a 504 designation.
  • •History of concussion less than 6 months to the study participation
  • •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.

研究组 & 干预措施

Normative

Other

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

干预措施: Normative (Device)

Reliability

Other

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

干预措施: Reliability (Device)

结局指标

主要结局

Validity

时间窗: 12 months

ImPACT Touchscreen performs within normal parameters of ImPACT Online

次要结局

  • Reliability(Baseline test will be administered at enrollment and re-test will be administered within 60 days of baseline test.)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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