Reliability and Validity of a New Device Measuring Spinal Rotation on the Transverse Plane
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Οne cohort of participants will be used and the reliability of the equipment will be used to test/retest the repeatability of the measurements
The validity will be measured against a gold standard for measuring angles
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Georgios Krekoukias, PT, PhD
- Phone Number: +306934609400
- Email: gkrekos@gmail.com
Study Contact Backup
- Name: Vasiliki Kalidoni
- Phone Number: +306937647333
- Email: vkalidoni19@gmail.om
Study Locations
-
-
Attica
-
Athens, Attica, Greece, 11471
- Recruiting
- Motus Liberi Physiotherapy Centre
-
Contact:
- GEORGIOS KREKOUKIAS, PT, PhD
- Phone Number: 6934609400
- Email: gkrekos@gmail.com
-
Contact:
- Vasiliki Kalidoni, PT
- Phone Number: +306937647333
- Email: vkalidoni19@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria: lumbar and thoracic scoliosis -
Exclusion Criteria: recent spinal surgery, cancer, spinal fixation
-
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reliability
Time Frame: 2021-2022
|
Reliability of device on repeated measures both intra and inter observer
|
2021-2022
|
|
Validity
Time Frame: 2021-2022
|
Validity of device will be measured
|
2021-2022
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Study Chair: Konstantinos Soultanis, MD, Attikon University Hospital, Athens, Greece
- Principal Investigator: GEORGIOS KREKOUKIAS, PT, PhD, PT, PhD
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 18221
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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