Robots map how brain and nerve injuries disrupt everyday arm tasks
NCT ID NCT02778529
First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time
Summary
Researchers at the University of Pennsylvania are studying how people with stroke, upper limb amputation, spinal cord injury, or cerebral palsy move their arms during common daily activities like drinking and pouring. The study uses two passive desktop robots to track the motion of each arm in participants and healthy volunteers. By comparing movement patterns, the team aims to understand how damaged nerve pathways affect the ability to perform everyday tasks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bilateral assessment robots (BiAS), two passive desktop robots that measure arm movement
- What this could lead to
- If the robot measurements reveal clear movement patterns, this could help therapists design better rehabilitation plans for people with long-term arm impairments.
- What could go wrong
- The study is small, with only 18 participants, and it does not test any treatment. The findings may not apply broadly, and measuring movement in a lab may not reflect real-world abilities.
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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18 people
The number who actually took part.
- Started
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May 2014
- Finished
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Sep 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: Study will include subjects 18 years of age or older from any of the below groups: * Stroke survivors, 3 months post event * Upper extremity amputees, 3 months post event * Cervical SCI (C-5 to C-7), 3 months post event * Cerebral palsy participants * Healthy participants Exclusion Criteria: * The inability to perform at least some aspects of ADL tasks such as drinking, pouring, pinching, and grasping. * Severe spasticity
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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
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Penn Medicine Rittenhouse
Philadelphia, Pennsylvania, 19146, United States
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