Wearable device aims to track MS progression from home
NCT ID NCT06346704
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
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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 Hide 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
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Other studies related to the condition(s) this trial covers.
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