Smartwatches and video exams: a new way to predict MG Flare-Ups?

NCT ID NCT07787247

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time

Summary

This pilot study explores whether continuous monitoring with wearable devices and remote neurological exams can detect worsening in people with myasthenia gravis (MG), a condition causing fluctuating muscle weakness. The goal is to see if this technology is reliable and if patients can stick with it for 12 months. If it works, it might help catch flare-ups early and avoid hospital visits.

What this could mean

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

Active substance
Remote monitoring program using wearable devices (e.g., Fitbit) and telemedicine-based neurological exams
What this could lead to
If successful, this approach could enable earlier detection of MG worsening, potentially reducing hospitalizations and emergency treatments.
What could go wrong
This is a small pilot study focused on feasibility, not effectiveness. The technology may not reliably predict flare-ups, and patient compliance could be low.

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 18 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Oct 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.

Who is studied

Myasthenia Gravis Patients who satisfy the study's eligibility criteria

Ages

18 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: Subject 1. Has the capacity to understand and sign an informed consent form 2. ≥18 years old 3. Diagnosed with acquired autoimmune MG based on clinical syndrome and seropositivity for MG associated autoantibodies (AChR binding, MuSK, or LRP4 antibodies), and/or a decremental response on repetitive nerve stimulation, positive single fiber electromyography (EMG) or positive edrophonium test 4. Subject has been previously evaluated in a face-to-face clinical encounter at participating study site or referral site within the prior 3 years 5. Primary language is English, or equivalent level of English language fluency 6. Required disease severity range previously judged by the Investigator. MGFA class 1-4a within 3 years of diagnosis without other chronic medical conditions, which compromise participation. 7. Having MG-ADL score above 2 upon entrance to study 8. Patients considered by study PI not to require hospitalization at time of entrance 9. The patient has internet capability and a smart phone compatible with the apps required by the study. Exclusion Criteria: Disease Specific Exclusion Criteria 1. Inability to comply with study protocol for monitoring 2. Current MGFA Severity Class IVb or V, or patients in remission with MGFA Class 0 3. Any significant medical/psychiatric condition that, in the opinion of the Investigator, may interfere with interpretation of subject evaluation(s) or protocol compliance 4. Any disorder that could limit ability to assess myasthenia gravis specific deficits (not including planned or recent thymectomy) 5. Pregnancy, based on the evaluator's judgment, if the subject is deemed not safe to undergo evaluation or comply with study visit requirements. 6. Lack of effective internet connection or ability to use study telemedicine station and monitors 7. Home environment prevents use of study equipment 8. Likelihood of leaving DC, Maryland, or Virginia area in year after initiation of study 9. Subject is already participating in a research study -

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Myasthenia gravis (MG) are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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 ↗

  3. 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.

Contacts and locations

Locations

  • The George Washington University

    RECRUITING

    Washington D.C., District of Columbia, 20037, United States

More trials for these conditions

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