MEVA Cognitive Wellness Platform Study for Adults (NCT07595250) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
MEVA Cognitive Wellness Platform Study for Adults
100 participantsStarted 2026-05
Plain-language summary
The goal of this observational study is to evaluate the reliability, usability, and feasibility of the MEVA Cognitive Wellness Platform in community-dwelling adults aged 55 to 75.
The main questions it aims to answer are:
How consistent is the MEVA Global Cognitive Index when participants complete the MEVA activities again approximately 14 days later? How usable and acceptable is the MEVA platform for older adults in community settings? What completion rates, data quality patterns, and participant feedback are observed during use of the platform?
Participants will:
Complete a baseline study visit lasting approximately 45 to 60 minutes Complete a 7-activity digital cognitive wellness battery Answer questionnaires about usability, technology acceptance, and wellness experience Complete the Saint Louis University Mental Status (SLUMS) examination as an exploratory comparison measure If selected for the retest group, return approximately 14 days later to complete the MEVA activities again
MEVA is being evaluated as a cognitive wellness platform. It is not intended to diagnose, treat, prevent, screen for, or monitor any disease or medical condition.
Who can participate
Age range
55 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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 br…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Test-retest reliability of the MEVA Global Cognitive Index
Timeframe: Baseline (Visit 1) and retest approximately 14 days later (Visit 2, allowed window 11-17 days)