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Wearable device aims to track MS progression from home

NCT ID NCT06346704

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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a wearable device called Syde® in 86 people with multiple sclerosis. Participants wore the device for one month every six months over two years. The goal was to see if the device's activity data matches standard clinic tests like walking speed and disability scores. The study was terminated early, so results may be incomplete.

What this could mean

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

Active substance
Syde® wearable device
What this could lead to
If successful, this could provide a new way to track multiple sclerosis progression at home using a simple wearable device.
What could go wrong
This is an early observational study that was terminated, so results may be limited. The device may not accurately reflect disease status or replace standard clinical assessments.

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

86 people

The number who actually took part.

Started

Apr 2024

Finished

Apr 2025

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

Subjects followed for multiple sclerosis care at the investigational site.

Ages

18 to 65 years

Sex

Anyone

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: 1. Male or female subject aged from 18 to 65 years old. 2. Signed informed consent and ability to comply with study and follow-up. 3. Diagnosed with MS base on 2017 McDonald criterion 4. EDSS ≤ 5.5 5. No clinical or radiological relapse within the last 3 months 6. For patient under treatment, the molecule and its dose should be stable about 2 months before inclusion 7. Subject willing and able to comply to all study procedures including the Syde® related ones Exclusion Criteria: 1. Patient with a cognitive or communicational disorder disturbing the understanding of the tasks or data collection 2. Previous or current disorder with an impact on current ambulation or motor function 3. Patient who have had surgery or traumatic injury in upper or lower limb within the last 6 months before the inclusion or patients who have had major surgery or trauma within the last 6 months before the inclusion

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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.

Contacts and locations

Locations

  • Air Force Specialized Hospital

    Cairo, Egypt

More trials for these conditions

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