Wearable motion sensor(s) to measure change of physical function in patients after total knee replacement.
- Conditions
- totale knie vervangende operatiekneeprosthesistotal knee replacement10023213
- Registration Number
- NL-OMON45809
- Lead Sponsor
- Imec Nederland
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 25
- patient with knee osteoarthritis undergoing primary total knee replacement of one knee within 3 months.
- age > 18 years
- informed consent
- willing to travel to hospital for 3 additional visits
a) Subjects with an artificial joint/limb in the lower body.
b) Subjects diagnosed with and/or taking medication for any musculoskeletal, neurological disorder or inflammatory arthritis.
c) Subjects who are pregnant or likely to become pregnant
d) Subject with known allergy to adhesive Ag/AgCl electrodes
e) Subjects using medication with phototoxic side effects: Tetracylines, Doxycycline, Phenothiazines, Dacarbazine, Ketoprofen, Lomefloxacin. In order to exclude possible local skin irritation from prolonged irradiation by LED-light (from activity monitor).
f) Patients that do not want to be informed in case of incidental findings.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method