Robot harness study aims to improve rehab for spinal injury patients
NCT ID NCT03004144
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study looks at how a robotic body-weight support system called FLOAT affects the way people with incomplete spinal cord injury perform everyday tasks like walking, standing up, and climbing stairs. Researchers measure movement and muscle activity with and without the robot's help. The goal is to learn how to better tailor rehabilitation exercises for each patient.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- FLOAT body-weight support system
- What this could lead to
- If successful, this could help design better rehabilitation programs for people with spinal cord injury.
- What could go wrong
- This is a small, early-stage study focused on measuring movement, not testing a treatment. Results may not lead to direct benefits.
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
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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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65 people
The number who actually took part.
- Start date
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Oct 2016
- Finished
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May 2025
- 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: * Individuals with incomplete spinal cord injury (AIS C-D) or able bodied persons * informed consent as documented by signature * bodyweight \< 120 kg Exclusion Criteria: * a significant psychiatric or orthopedic diagnose * any secondary neurological complications that may impact the outcome variables * dermatological conditions (pressure ulcers, etc.) * pacemaker or other implanted, electronic devices * contraindications for FLOAT training * inability or unwillingness to provide written informed consent or follow study procedures e.g. due to language problems * psychological disorders, dementia, etc. * known or suspected non-compliance, drug or alcohol abuse * enrolment of the investigator, his/her family members, employees and other dependent persons
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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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Universitätsklinik Balgrist
Zurich, 8008, Switzerland
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Other studies related to the condition(s) this trial covers.
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