eg prosthesis to improve lateral balance
- Conditions
- unilateralprostheticsprototypePeaucellierbovenbeenamputatieeenzijdigprothesesPeaucellierabove knee amputation
- Registration Number
- NL-OMON24065
- Lead Sponsor
- 1) Department of Rehabilitation Medicine, UMCG2) SPRINT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
All subjects must be able to understand and follow spoken instructions in order to be included. Further, subjects must meet all of the following criteria:
Exclusion Criteria
A potential subject who meets any of the following self reported criteria will be excluded from participation in this study:
-Serious vascular problems or pain of the non-amputated limb;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method This is a pilot study. Therefore, no main outcome parameters can be specified. The goal of this study is however to validate a new prototype prosthetic device in terms of lateral balance control improvements. Therefore, our focus will be on finding improvements in lateral balance control of subjects wearing the prototype.
- Secondary Outcome Measures
Name Time Method