Assistive acting and bio-sensor-based self-adaptive motion supporting therapy device for individual treatment: clinical evaluatio
Not Applicable
- Conditions
- Z96.65
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Healthy subjects:
knee joint with minimum movement range of 0° - >90°; sufficient understanding of the German language
Patients after total knee arthroplasty:
>50 years; 1-3 weeks postoperativ after first time endoprosthetic treatment of the inspected knee; inpatient treatment in the rehabilitation fascility Federseeklinik Bad Buchau; sufficient understanding of the German language
Exclusion Criteria
Healthy subjects:
skin disease on the leg; knee pain; neurological disorders/psychological disorders; knee arthroplasty; artificial joint replacement of the ankle; cardiac pacemaker (due to possible leakage current)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Safety and security<br>Safety is assessed by means of a questionnaire developed in-house and qualitative interviews.
- Secondary Outcome Measures
Name Time Method