Brain training may boost memory after concussion, study suggests

NCT ID NCT03655782

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jun 26, 2026 · Last updated Jul 16, 2026 · Updated 2 times

Summary

This study tests whether 36 sessions of a computer-based brain training program, called PATH neurotraining, followed by digit memory exercises, can improve working memory, processing speed, and attention in people who have had a mild traumatic brain injury (concussion). The training involves watching moving patterns on a screen and pressing keys to report what was seen. The study includes 90 participants and measures changes in visual working memory and processing speed. The goal is to find a safe, non-drug way to help people recover cognitive skills after a concussion.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
PATH neurotraining and digit memory exercises
What this could lead to
If it works, this could provide a non-drug way to improve thinking and memory after a concussion.
What could go wrong
This is a small, early-phase study with only 90 participants, so results may not apply to everyone. The training requires many sessions, and benefits may vary.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 90 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2023

Expected to finish

Sep 2029

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 60 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Referred by Clinician verifying that patient has an mTBI (also includes moderate TBI: those who had a severe TBI with a loss of consciousness more than 30 minutes that is now an mTBI) and has a visual working memory loss as determined by first neuropsychological pre-test administered: The Test of Information Processing Skills (TIPS), 2. One or more concussions, 3. Any loss of consciousness from 5- 30 min (not longer than 30 min) to be in mTBI group, otherwise in moderate TBI group. 4. Any loss of memory for events immediately before or after the accident for 24 hours is in mTBI group, otherwise is in moderate TBI group, 5. Any alteration of mental state at the time of the accident (e.g. feeling dazed, disoriented, or confused), 6. Be between the ages of 18 to 60 years, when development and aging are not factors, 7. Agrees to complete the study after hearing the time commitment involved, 8. Has corrected 20/20 visual acuity, and normal motor control so can do PATH neurotraining (signal direction that dim gray stripes move by pushing arrow keys on the computer), 9. Can sign and understand the informed consent form themself, 10. Can drive to test sites or capable of using public transportation (bus or train) to test site. 11. Reads English fluently, so can follow instructions. Exclusion Criteria: 1. mTBI occurred less than 3 months earlier \[While post-concussive symptoms (PCS) resolve within days post injury in the majority of individuals with mTBI,127 symptoms can endure 3 months post injury or longer, indicating spontaneous recovery and chronic sequela.128 In the general public, between 8% to 33% of mTBI patients have persistent PCS and long-term cognitive and/or behavioral impairments129 that negatively impact quality of life. In the proposed study, we will try to minimize the confound from the spontaneous recovery by only recruiting chronic mTBI subjects, and not recruiting mTBI subjects with mTBI less than 3 months.\] with no maximum time if still experiencing memory problems which will be measured by the TIPS visual working memory (VWM) scores. 2. diagnosis of epilepsy or seizure disorder in last 12 months, 3. diagnosis of moderate depressive disorder or moderate anxiety, having driving limitations in traffic 4. answers 'Yes' to any of the questions on the Columbia Suicide Severity Rating Scale, 5. had a stroke or metabolic derangements causing cognitive impairments, i.e. alcohol or substance abuse, And for those chosen to undergo MEG exams: 6. has extensive metal dental hardware (e.g., braces and large metal dentures; fillings are acceptable) or other metal objects in head, neck, or face areas that cause artifacts in MEG data, and are not removable during pre-processing, and 7. has claustrophobia since MRI scanner is in small enclosed space, 8. has a cardiac pacemaker, or 9) is pregnant.

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Conditions

The condition(s) this trial relates to.

Brain Concussion traumatic brain injury

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Perception Dynamics Institute

    Solana Beach, California, 92075, United States

  • University of California at San Diego

    San Diego, California, 92121, United States

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