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Brain games before surgery: a new way to spot delirium risk?

NCT ID NCT06245005

What the study statuses mean

This study's is highlighted.

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether older adults (60+) scheduled for major surgery could complete a set of six brain exercise games on a tablet before their operation. The goal was to see if this was practical in a busy clinic or hospital setting and whether the first-time game scores could help predict who might experience confusion (delirium) after surgery. 120 participants were enrolled, and the researchers measured how many completed the games and how satisfied they were with the experience.

What this could mean

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

Active substance
Lumosity brain exercise games on a portable electronic device
What this could lead to
If successful, this could provide a quick, simple way to measure cognitive reserve in older surgical patients and help predict who might develop postoperative delirium.
What could go wrong
This is a small feasibility study, not designed to prove effectiveness. The brain games may not be practical in busy clinical settings, and results may not predict delirium reliably.

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.

Participants

120 people

The number who actually took part.

Started

Sep 2023

Finished

Jan 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Who is studied

Patients 60 years of age or older, capable and willing to consent and scheduled to undergo non-cardiac/non-neurological surgery with an expected hospital stay of at least 72 hours.

Ages

60 years and older

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. 60 years of age or older 2. Capable and willing to consent 3. Non-cardiac/non-neurological surgery with an expected hospital stay of at least 72 hours 4. Anticipated ASA physical status I-IV 5. English speaking 6. Willingness to use computer-based device Exclusion Criteria 1. Severe visual or auditory deficits 2. Illiterate 3. Surgery or procedure within the previous 6 months requiring general anesthesia 4. Active Axis I or II psychiatric disorders including bipolar disorder, schizophrenia, dementia, alcohol, or drug abuse 5. ASA physical status V, VI 6. Planned postoperative ICU admission 7. Preoperative benzodiazepine administration (i.e. Midazolam, Diazepam)

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Conditions

The condition(s) this trial relates to.

Cognitive Dysfunction

As listed by the trial registrant

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

Contacts and locations

Locations

  • The Ohio State University Wexner Medical Center

    Columbus, Ohio, 43210, United States

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Other studies related to the condition(s) this trial covers.