New brain wellness app under study – no diagnosis, just data
NCT ID NCT07595250
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
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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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
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55 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
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.
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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.
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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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