Smart socks for surgery recovery? wireless insole measures walking after hip or knee replacement
NCT ID NCT03673293
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a wireless insole device (Loadsol) in 58 people who had hip or knee replacement surgery. The goal was to see if the device could accurately measure how much weight they put on their leg while walking and if giving feedback could help improve their walking symmetry. The study was completed and focused on evaluating the technology, not on providing a new treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Loadsol wireless insole device
- What this could lead to
- If successful, this could provide a simple way to track recovery after joint replacement and help patients improve their walking symmetry.
- What could go wrong
- This is a small, completed study focused on measuring outcomes, not testing a treatment. The device may not prove useful for improving recovery in larger or more diverse groups.
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
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58 people
The number who actually took part.
- Started
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May 2018
- Finished
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Aug 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.
Who is studied
Patients who plan or recently underwent (up to 8 weeks postoperatively) primary total joint arthroplasty
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Planned or recently underwent (up to 8 weeks postoperatively) primary total joint arthroplasty * Free walking before surgery, no devices needed * Age \>/=18 years * Preoperative outcomes scores (PF CAT, PROMIS Global Health, KOOS JR) * Written informed consent Exclusion Criteria: * Index procedure is a revision total joint arthroplasty * Total knee or hip arthroplasty on the contralateral side within 1 one year of index procedure * Severe medical comorbidity (ASA\>/=3) * Participant is planning TJA on another joint within next 12 months * Significant symptoms on contralateral knee/hip/ankle that could impede performance on study
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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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University of Utah Orthopaedic Center
Salt Lake City, Utah, 84108, United States
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