Limited Market Release - MotionSense Clinical Use Evaluation
Completed · Not applicable
Conditions studied: Knee Arthroplasty, Patient Engagement, Patient-Reported Outcome Measures (PROMs)
In brief
Prospective evaluation of patient compliance and prescribed home exercise program using MotionSense wearable system during recovery from primary total knee arthroplasty.
Key facts
- Study ID
- NCT05091918
- Run by
- Orthosensor, Inc.
- People needed
- 101
- Starts
- 2021-05-27
- Expected to finish
- 2022-08-01
- Last updated by the study team
- 2024-07-10
Who can join
Age: 50 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Planned for unilateral total knee surgery in the coming 4 weeks
- Age 50 to 80
- Owns a smart phone
You may not qualify if…
- BMI exceeding 35
- Severe skin conditions
Where it is running
- Oklahoma Joint Reconstruction Institute — Oklahoma City, Oklahoma, United States
- Robotic Joint Replacement Institute LLC — Wakefield, Rhode Island, United States
Full record on ClinicalTrials.gov
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