Validity of the Kinect™ Sensor for Measuring Range of Motion in Patients Post-stroke and Healthy Test Subject
试验速览
- 阶段
- 不适用
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- 3D kinematic measurements upper limb
研究概览
简要总结
The aim of this research is to investigate the validity of the Kinect™ 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).
详细描述
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. 2. The Kinect system
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •People post-stroke or healthy test subjects
- •Language: Dutch, English or French
- •Able to sit and stand unsupported for 30 s or more
- •Able to stand up from a chair without aid of another person
- •Able to signal pain, fear of discomfort
- •Able to give informed consent (based on the advice of a medical doctor)
- •Able to understand and perform the instructions and to answer questions
排除标准
- •Concurrent orthopedic and/or musculoskeletal pathologies or disorders that may limit the range of motion (including limb amputations)
- •Concurrent neurological disorders (e.g. Parkinson's Disease, Multiple Sclerosis or Amyotrophic Lateral Sclerosis)
- •Persons with comorbidity that could hinder the study (e.g. unstable cardiovascular system disorders, lung disorders, severe osteoporosis)
- •People with difficulties of speech and/or memory providing that instruction cannot be followed or understood adequate
研究组 & 干预措施
Kinect validation
Kinect measurements will be compared with the vicon measurements to validate the kinect system.
干预措施: Kinect validation (Other)
结局指标
主要结局
3D kinematic measurements upper limb
时间窗: through study completion, an average of 1 year
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.
3D kinematic measurements lower limb
时间窗: through study completion, an average of 1 year
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.
次要结局
未报告次要终点
研究者
Emma De Keersmaecker
Principal Investigator
Vrije Universiteit Brussel