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Your voice may reveal hidden exhaustion: new study tests AI fatigue detection

NCT ID NCT07033559

What the study statuses mean

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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.
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
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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 Results may not be published yet.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

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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This observational study will test whether computer analysis of voice recordings can detect a deep type of exhaustion called central fatigue in people with generalised myasthenia gravis. 240 adults in the US and UK will record themselves speaking twice daily, twice a week for 4 weeks, and answer short questionnaires. The goal is to see if voice patterns can reliably signal fatigue, potentially enabling remote monitoring.

What this could mean

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

What this could lead to
If successful, this could lead to a simple, remote way to monitor fatigue in myasthenia gravis using just a voice recording.
What could go wrong
This is an early observational study, not a treatment trial. The voice analysis may not be accurate enough, or patients may find daily recordings burdensome.

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 240 people

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

Expected to start

Feb 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

The study population consists of a convenience sample of adults with generalised Myasthenia Gravis recruited through a decentralised, multi-channel approach across the United States and United Kingdom. This remote recruitment strategy leverages established myasthenia gravis patient networks, charities and digital platforms like social media groups to reach geographically dispersed participants. The decentralised methodology is particularly appropriate for studying a rare condition where patients may have limited mobility due to fatigue and muscle weakness.

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: * Adults ≥18 years old * Self-reported generalised Myasthenia Gravis diagnosis confirmed by healthcare provider for ≥6 months * Disease stability for ≥6 months (no hospitalisations, medication changes, or significant symptom worsening) * English as first language * Residence in US or UK * Vision adequate for screen reading (with aid or correction if necessary) * Access to internet-connected device with compatible browser and microphone * Adequate internet connectivity (≥5 Mbps download, ≥3 Mbps upload) * Ability to complete twice-daily assessments during specified time windows * Signed electronic informed consent Exclusion Criteria: * Pure ocular Myasthenia Gravis * Diagnosed mild cognitive impairment or dyslexia * Speech or hearing impairments affecting voice recording * Unable to provide credible diagnostic information (healthcare provider diagnosis, antibody test results, current medications) * Major inconsistencies in reported medical history * Unsigned informed consent

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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How to take part

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  1. The official record

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