Can a High-Tech sleeve match standard arm measurements?
NCT ID NCT07074483
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a wearable device called AuReha can measure arm movements as accurately as the usual method (a goniometer). 96 healthy volunteers performed exercises while wearing the device and being measured with standard tools. The goal was to see if the wearable could be a reliable alternative for tracking rehabilitation progress.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AuReha wearable device (sensorized garment for upper limb movement measurement)
- What this could lead to
- If successful, AuReha could provide a more convenient way to track arm movements during rehabilitation, potentially improving home-based therapy.
- What could go wrong
- This is an early validation study in healthy people, not patients. It does not test any treatment or health outcome, so real-world benefits are uncertain.
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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96 people
The number who actually took part.
- Started
-
Jun 2025
- Finished
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Dec 2025
- Lead sponsor
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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.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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: * Age \> 18 years * Volunteers who provide written informed consent to participate in the study * Absence of movement limitations affecting the upper limbs and/or trunk Exclusion Criteria: * Pregnant and/or breastfeeding women (verified through self-declaration) * Epilepsy * Allergy or hypersensitivity to materials used in the medical device, specifically: polypropylene and lycra (fabric), nylon (integrated zipper), viscose and elastane (zipper integration fabric) * Chronic headache under treatment
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
IRCCS Ospedale Galeazzi - Sant'Ambrogio
Milan, Italy, 20157, Italy
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