Risk Screening and Assessment of Shoulder, Neck and Lower Back Discomfort.
试验速览
- 阶段
- 不适用
- 入组人数
- 300
- 试验地点
- 1
- 主要终点
- Oswestry Disability Index (ODI)
研究概览
简要总结
Identifying high-risk factors that may lead to shoulder, neck and lower back discomfort and contributing to the primary prevention of disease progression.
详细描述
The purpose of this study is to design a self-assessment scheme for clinical assessment of shoulder, neck and lower back function and compare the consistency between clinical assessment and self-assessment. The body parameters (BMI, age, gender), daily activities (daily steps, sedentary), work and rest time (sleep time, quality) were collected through wearable devices, evaluating the risk factors of shoulder, neck and lower back discomfort.
研究设计
- 研究类型
- Observational
- 观察模型
- Ecologic Or Community
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 20 Years 至 40 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Oswestry Disability Index (ODI)
时间窗: at least 2-week monitoring by wearable devices
Oswestry Disability Index of the neck is collected for the evaluation of neck functions.
Roland-Morris Disability Questionnaire (RDQ)
时间窗: at least 2-week monitoring by wearable devices
Roland-Morris Disability Questionnaire is collected for the evaluation of lower back functions.
Range of motion (ROM) of the neck
时间窗: at least 2-week monitoring by wearable devices
Patients' range of motion of the neck in all directions are measured using hand-held devices.
Visual Analogue Scale (VAS)
时间窗: at least 2-week monitoring by wearable devices
Visual Analogue Scale is collected for pain assessment.
次要结局
未报告次要终点