QUANTIFYING PROSTHESIS ALIGNMENT IN TRANSTIBIAL BONE-ANCHORED PROSTHESIS USERS

Recruiting

Conditions: Bot-verankerde prothesegebruikers
bone-anchored prosthesis
Osseointergration

Registration Number: NL-OMON52260

Lead Sponsor: Radboudumc Nijmegen

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Not specified

Target Recruitment: 27

Inclusion Criteria

Persons will be eligible for the study if they use a unilateral trans-tibial
bone-anchored prosthesis for at least one year. They need to be able to walk
without additional assistive devices during the measurements. An activity level
of K3-K4 is required and all participants should be over 18 years of age.

Exclusion Criteria

Persons with cognitive or communicative limitations or visual limitations as
well as physical co-morbidity, that would hinder smooth locomotion and save
locomotion during the measurements, will be excluded from participation in this
study .

Study & Design

Study Type: Observational invasive

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The level of symmetry in moments around the hip and knee between the residual<br /><br>limb and the sound limb. This data will be collected at self-selected<br /><br>comfortable walking speed, and we will compare baseline alignment condition to<br /><br>the WBL alignment condition within the participants.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Investigating the relationship between a structural change in alignment and the<br /><br>change in knee, hip and implant moments in trans-tibial bone-anchored<br /><br>prosthetic users in the frontal plane. Thereby, we investigate if the<br /><br>weight-bearingline alignment method results in short term (within 2 weeks)<br /><br>physical complaints</p><br>