New brain wellness app under study – no diagnosis, just data

NCT ID NCT07595250

Knowledge-focused Sponsor: Mentage LLC Source: ClinicalTrials.gov ↗

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study will test a digital platform called MEVA that measures cognitive wellness in healthy adults aged 55 to 75. Participants will complete activities and questionnaires to see how reliable and easy the platform is. The goal is to understand if the tool works well for older adults living in the community. This is not a treatment or diagnostic study.

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

About 100 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

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.

Who is studied

Community-dwelling adults aged 55 to 75 years who are generally healthy or have stable chronic conditions and are interested in cognitive wellness research. Participants are recruited through community-based outreach, including senior centers, libraries, faith-based organizations, wellness programs, and word of mouth. Recruitment is designed to support demographic and socioeconomic diversity.

Ages

55 to 75 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Adults aged 55 to 75 years * Community-dwelling (living independently in the community) * English fluency sufficient for informed consent, task instructions, and questionnaires * Able to provide informed consent using teach-back method * Able to use a computer or tablet for simple tap or drag interactions * Functional vision sufficient for on-screen tasks with usual corrective lenses * Functional hearing sufficient for spoken instructions with or without hearing aids * Interest in cognitive wellness and personal well-being * Available for baseline visit and possible retest visit approximately 14 days later * Transportation to study site or ability to participate remotely if permitted by protocol * Assistive devices and accommodations are permitted Exclusion Criteria: * Severe visual impairment preventing completion of digital tasks * Severe motor impairment preventing interaction with tablet or web application * Known diagnosis of moderate or severe dementia, or inability to comprehend consent and task instructions * Current participation in another cognitive training or technology intervention study likely to confound outcomes * Recent hospitalization, emergency room visit, or acute exacerbation of a medical or psychiatric condition within the past 30 days that would impede study participation * Current substance use disorder likely to interfere with study adherence or completion * Recent intensive use of a similar structured cognitive wellness or brain training application

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Conditions

The condition(s) this trial relates to.

cognitive disorder Health Behavior

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

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