Ignite Creation Date:
2025-12-24 @ 7:51 PM
Ignite Modification Date:
2025-12-25 @ 5:27 PM
Study NCT ID:
NCT02134704
Status:
TERMINATED
Last Update Posted:
2016-08-30
First Post:
2014-05-05
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
MOUVSCO: Kinematic Analysis of the Trunk in Patients With Moderate Scoliosis
Sponsor:
University Hospital, Grenoble
Organization:
Study Overview
Official Title:
Kinematic Analysis of the Trunk in Patients With Moderate Scoliosis
Status:
TERMINATED
Status Verified Date:
2016-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
All patients were recruted but it has been difficulte to recrute all volunteers (15/30) . However data should be sufficient for analyse of data.
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MOUVSCO
Brief Summary:
The hypothesis of this study is that moderate scoliosis patients have postural and kinematic differences (static and dynamic) compared with healthy volunteers and it is possible to characterize and quantify.
The aim of this study is the detailed analysis of postural anomalies in moderate scoliosis patients compared with healthy volunteers
The aim of this study is the detailed analysis of postural anomalies in moderate scoliosis patients compared with healthy volunteers
Detailed Description:
Subjects participating in the study must wear sensors that will be arrange at the shoulders, spine, pelvis and legs. Subjects will perform under the direction of the investigator, different tasks of a total duration of 45 minutes.
During the period of experimentation, the data collected will be:
* the positions of each one of the sensors in all three planes of space,
* the ground support forces
During the period of experimentation, the data collected will be:
* the positions of each one of the sensors in all three planes of space,
* the ground support forces
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?: