Wearable tech takes on knee injuries: small study tests sensor accuracy
NCT ID NCT03805464
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a wearable sensor can detect changes in knee joint loading after a small amount of fluid is injected into the knee (simulating injury). Fourteen healthy adults aged 18-35 participated. Researchers measured walking patterns, muscle activity, and balance before and after the injection. The goal was to see if an inexpensive, publicly available sensor could spot biomechanical changes, which could help monitor knee injuries and osteoarthritis in the future.
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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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14 people
The number who actually took part.
- Started
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Jan 2019
- Finished
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May 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 to 35 years
- 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: * Male and female * Chronological age 18-35 at the time of study participation * Physically active (at least 30 minutes of physical activity, 3x/week) * Tegner Activity Scale score at least 5/10 Exclusion Criteria: * History of lower extremity or lumbar spine surgery. * History of lower extremity or lumbar spine injury in the prior 6 months. * History of major ligamentous damage. * Current knee pain. * Known neurological condition, autoimmune condition, cardiovascular disease. * History of epilepsy, seizures, concussion within the prior 6 months. * Currently taking pain altering medication. * Fear of needles * Unable to read and understand English language * Pregnancy
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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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Michael W. Krzyzewski Human Performance Laboratory
Durham, North Carolina, 27705, United States
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Other studies related to the condition(s) this trial covers.
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