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App aims to empower older adults with memory challenges to master medication routines

NCT ID NCT07754994

Symptom relief Sponsor: University of Illinois at Urbana-Champaign 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 10, 2026 · Last updated Aug 11, 2026 · Updated 1 time

Summary

This study tests a mobile app called bpMedManage-R designed to help older adults with mild cognitive impairment who live alone manage their hypertension medication. Participants will use the app to set reminders and track their daily and weekly medication intake, with weekly check-ins from the research team. The goal is to see if the app improves their ability to take medications as prescribed and boosts their confidence in managing their health independently.

What this could mean

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

Active substance
bpMedManage-R mobile health application
What this could lead to
If effective, this app could help older adults with mild cognitive impairment manage their blood pressure medication more confidently and consistently, potentially reducing health risks.
What could go wrong
This is a small feasibility study, so results may not be conclusive. The app's success depends on user engagement and may not work for everyone.

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 40 people

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

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Jun 2028

An estimate. End dates often move.

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.

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: * Age 60+ * Fluent in English * Adequate visual and auditory acuity * Community dwelling * Lives alone * Self-reported memory problems * Manage at least one hypertension medication * Passing score on Telephone Interview for Cognitive Status - Modified (TICS- M) between 27-37 * Passing score on Montreal Cognitive Assessment (MoCA) between 20 and 26 * Geriatric Depression Scale (GDS) score of 6 or lower * Stated willingness to comply with all study procedures and availability for the duration of the study Exclusion Criteria: * Diagnosis of dementia * Major communication difficulties

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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.

Mild cognitive impairment (MCI)

How to take part

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

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    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.

More trials for these conditions

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