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Could a sleep monitor help ALS patients breathe easier?

NCT ID NCT07502677

First seen Apr 03, 2026

Summary

This study tests whether a wearable device called SleepImage can accurately detect respiratory failure in people with ALS (Lou Gehrig's disease). Researchers will compare the device's readings with standard overnight sleep tests in 15 patients. The goal is to find a simpler way to decide when to start non-invasive ventilation (breathing support), potentially improving quality of life and care timing.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Royal Brompton Hospital

    RECRUITING

    London, sw3 6np, United Kingdom

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

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

Active substance

SleepImage device (wearable sleep monitor)

What this could lead to

If successful, this could provide a simpler, home-based way to detect when ALS patients need breathing support, potentially improving timing of care.

What could go wrong

This is a very small early study (15 people) testing a device, not a treatment. The device may not be accurate enough, and results may not apply to all ALS patients.

Conditions

The condition(s) this trial relates to.

amyotrophic lateral sclerosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.