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ImPACT Touchscreen Assessment for Concussion

N/A
Waitlist Available
Research Sponsored by ImPACT Applications, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights

Study Summary

This trial will help researchers understand how well the ImPACT concussion-monitoring tool works on touchscreen devices, which could help more people get access to concussion screening.

Who is the study for?
This trial is for English-speaking adolescents and adults aged 12 to 80 who have not had a concussion in the last six months. It's not suitable for those with special education needs (except a 504 designation), visual impairments that glasses can't correct, or psychological conditions like ADHD that could affect test performance.Check my eligibility
What is being tested?
The study aims to create a standard database and check the consistency of ImPACT, which is a tool used on touchscreen devices to assess cognitive changes possibly caused by concussions.See study design
What are the potential side effects?
Since this trial involves assessment tools rather than medical treatments, there are no direct side effects related to medications. However, participants may experience fatigue or stress while taking the tests.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Validity
Secondary outcome measures
Reliability

Trial Design

2Treatment groups
Experimental Treatment
Group I: ReliabilityExperimental Treatment1 Intervention
ImPACT will be administered to participant's within 60 days of baseline test.
Group II: NormativeExperimental Treatment1 Intervention
ImPACT will be administered to participant's for a baseline test.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Reliability
2023
N/A
~150

Find a Location

Who is running the clinical trial?

ImPACT Applications, Inc.Lead Sponsor
3 Previous Clinical Trials
2,800 Total Patients Enrolled

Media Library

Normative Clinical Trial Eligibility Overview. Trial Name: NCT05551520 — N/A
Concussion Research Study Groups: Normative, Reliability
Concussion Clinical Trial 2023: Normative Highlights & Side Effects. Trial Name: NCT05551520 — N/A
Normative 2023 Treatment Timeline for Medical Study. Trial Name: NCT05551520 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many participants are accepted in this research initiative?

"Affirmative. Clinicaltrials.gov contains information that confirms the ongoing recruitment of participants for this study, which was initially posted on February 7th 2022 and recently updated on September 20th 2022. This medical trial requires approximately 900 patients to be enrolled from 1 site."

Answered by AI

Does this research program have any open vacancies for participants?

"Affirmative, the information available on clinicaltrials.gov attests to this trial's active recruitment status. This project was initially posted on February 7th 2022 and most recently modified on September 20th 2022; with a goal of 900 participants at 1 research site."

Answered by AI

Does the age requirement for this research preclude those under 25 years old?

"The age range for this trial is 12-80 years old. There are 3 additional trials open to minors, and 2 studies specifically targeting the elder population."

Answered by AI

Am I eligible to participate in the experiment?

"Potential participants for this concussion trial must range in age from 12 to 80 and 900 applicants are being sought."

Answered by AI

Who else is applying?

What state do they live in?
New Mexico
What site did they apply to?
ImPACT Applications, Inc.
What portion of applicants met pre-screening criteria?
Met criteria
How many prior treatments have patients received?
0
~53 spots leftby Jun 2024