Comparison of the immobilizing effect of different neck orthoses
Recruiting
- Conditions
- Volunteer healthy participants (m/f/d) without known pre-existing conditions, pain, or movement restrictions in the cervical spine.
- Registration Number
- DRKS00033571
- Lead Sponsor
- niversitätsklinik Leipzig
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Volunteer healthy participants (m/f/d)
- Written consent declaration
Exclusion Criteria
- Pre-existing conditions, pain, or movement restrictions in the cervical spine
- Known allergy to any of the materials used in the manufacture of neck orthoses
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mobility of the cervical spine (flexion/extension/rotation/lateral flexion) measured in degrees.<br><br>1) Participants who meet the inclusion criteria are contacted via email or in person and informed about the planned study.<br>2) Optical markers are placed on the head of each participant using a headband.<br>3) Using multiple cameras and a digital image correlation system (Limess Meßtechnik und Software GmbH, Krefeld, Germany; ISTRA 4D Dantec Dynamics A/S, Skovlunde, Denmark), the maximum active flexion, extension, rotation, and lateral bending to the right and left are measured under the following conditions:<br>- without orthosis<br>- with soft orthosis<br>- with semi-rigid orthosis<br>- with rigid orthosis
- Secondary Outcome Measures
Name Time Method