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The aim of this research is to investigate the validity of the Kinectâ„¢ sensor in post-stroke patients and in healthy test subjects during analytic and functional movements. Measurements will be compared with the Vicon-camera system (currently seen as the golden standard).
STUDY DESIGN
This study is a cross-sectional study in which healthy people and people post stroke will perform 1 session where we will investigate the validity of the Kinect sensor.
MATERIALS
The VICON system
The Vicon Camera system is a marker-based system (MBS) to evaluate and analyse movements. Markers are placed on predetermined locations on the skin of the patient according to the Plug in Gait (PIG) full body model. Examination will take place in underwear. A 14-camera infrared opto-electronic video-based motion analysis system with a sample rate of 100 Hz (Vicon MX T40-S, Vicon Motion Systems, Oxford, UK) is used as golden standard. Two synchronized video cameras (Bonita 720C, Vicon, UK) will film the front and side of the participants at a sample rate of 100 Hz.
The Kinect system
The Kinectâ„¢ system is a markerless-system. It uses a skeleton model to estimate the joint and relative segment orientations. The Kinect-camera will be placed on a tripod at 1,5m height and patients will stand 2m from the camera as recommended by the manufacturer The Kinectâ„¢ Azure is the newest version of this system and will be used in this study.
PROCEDURE
All participants will be informed about the study (information document) and a confirmed written informed consent will be obtained by each participant. Baseline demographic and/or clinical characteristics from participants will be obtained by questioning and by searching medical files.
The participant will perform following analytical movements bilateral, both in sitting and standing position:
Hip:
Knee:
Shoulder:
Elbow:
The following functional movements will be performed:
Participants will perform 5 repetitions per movement, with 2 seconds between every repetition. Each side is moved separately.
If necessary, for safety reasons, the participant can use a walking aid to maintain the balance (e.g. rollator, crutch, …).
STATISTICAL ANALYSIS
Statistical analysis will be performed using SPSS version 23 (IBM, Chicago, IL). Significance will be set at 5%. The statistical analysis will be performed by the investigators.
To determine the validity, intraclass correlation coefficients will be calculated. Based on the 95% confidence intervals of the ICC estimates, agreement will be rated poor (less than 0.50), moderate (between 0.50 and 0.75), good (between 0.75 and 0.90) or excellent (greater than 0.90). Mean differences and standard deviations will also be calculated and interpreted.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Kinect validation | Experimental | Kinect measurements will be compared with the vicon measurements to validate the kinect system. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Kinect validation | Other | Participants will perform several movements while both the vicon and kinect are measuring. |
|
| Measure | Description | Time Frame |
|---|---|---|
| 3D kinematic measurements lower limb | Kinematic data (i.e. movement amplitudes of the bilateral hip, knee and ankle joint in degrees) of the lower limbs during the movements will be recorded continuously with the use of the VICON Vero 1.3 system at 100 Hz. | through study completion, an average of 1 year |
| 3D kinematic measurements upper limb | Kinematic data (i.e. movement amplitudes of the head, neck, spine, thorax and bilateral shoulder, elbow and wrist joint in degrees) of the lower limbs during the movements will be recorded continuously with the use of the VICON Vero 1.3 system at 100 Hz. | through study completion, an average of 1 year |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Eva Swinnen, Prof. Ph.D | Contact | 003224774527 | eva.swinnen@vub.be | |
| Emma De Keersmaecker | Contact | 003224774527 | emma.de.keersmaecker@vub.be |
| Name | Affiliation | Role |
|---|---|---|
| Eva Swinnen, Prof. Ph.D | Vrije Universiteit Brussel | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Brubotics Rehabilitation Research Center | Recruiting | Brussels | 1090 | Belgium |
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| ID | Term |
|---|---|
| D020521 | Stroke |
| ID | Term |
|---|---|
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |