Action Observation in Knee Replacement
- Conditions
- Total Knee Replacement
- Interventions
- Device: Control groupDevice: Experimental groupDevice: Conventional physiotherapy
- Registration Number
- NCT02707419
- Lead Sponsor
- Fondazione Don Carlo Gnocchi Onlus
- Brief Summary
Postoperative rehabilitation is required for a successful outcome following total knee arthroplasty. Traditionally rehabilitative programs aim to increase range of motion, to strengthen quadriceps, to restore normal gait, and to recover independence in activities of daily living. In the last decade action observation treatment, in addition to conventional physiotherapy has been proposed as a treatment method in rehabilitative medicine. There is growing evidence of the applicability of action observation training in rehabilitative medicine, indeed it has been applied in the rehabilitation of stroke of Parkinson disease of cerebral palsy and of aphasia.
Nevertheless those are small studies and one of them included a mixed population of hip and knee arthroplasty.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 41
- Primary total knee replacement.
- bilateral knee replacement
- previous total knee replacement.
- pre-existing motor impairment (i.e. hemiparesis, poliomyelitis, lumbar sciatica);
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Control group Conventional physiotherapy Video of nature scenes and conventional physiotherapy. 45 minutes twice a day, 5 days a week for 2 weeks. Experimental group Conventional physiotherapy Video of the exercises and conventional physiotherapy. 45 minutes twice a day, 5 days a week for 2 weeks. Control group Control group Video of nature scenes and conventional physiotherapy. 45 minutes twice a day, 5 days a week for 2 weeks. Experimental group Experimental group Video of the exercises and conventional physiotherapy. 45 minutes twice a day, 5 days a week for 2 weeks.
- Primary Outcome Measures
Name Time Method Change of Range Of Motion Baseline and immediately post-intervention Active and passive range of motion of knee
Change of Pain intensity Baseline and immediately post-intervention Visual Analogue Scale
- Secondary Outcome Measures
Name Time Method Barthel index Baseline and immediately post-intervention Barthel index
Short Form-36 motor Baseline and immediately post-intervention Tinetti scale Baseline and immediately post-intervention Lequesne index Baseline and immediately post-intervention
Trial Locations
- Locations (1)
Jorge Hugo Villafañe
🇮🇹Piossasco, Turin, Italy