Identifying high-risk factors that may lead to shoulder, neck and lower back discomfort and contributing to the primary prevention of disease progression.
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.
Study Type
OBSERVATIONAL
Enrollment
300
The body parameters (BMI, age, gender), daily activities (daily steps, sedentary), work and rest time (sleep time, quality) were collected through wearable devices. The range of motion of neck and waist was collected through hand-held devices.
Peking University Third Hospital
Beijing, China
RECRUITINGRange of motion (ROM) of the neck
Patients' range of motion of the neck in all directions are measured using hand-held devices.
Time frame: at least 2-week monitoring by wearable devices
Oswestry Disability Index (ODI)
Oswestry Disability Index of the neck is collected for the evaluation of neck functions.
Time frame: at least 2-week monitoring by wearable devices
Visual Analogue Scale (VAS)
Visual Analogue Scale is collected for pain assessment.
Time frame: at least 2-week monitoring by wearable devices
Roland-Morris Disability Questionnaire (RDQ)
Roland-Morris Disability Questionnaire is collected for the evaluation of lower back functions.
Time frame: at least 2-week monitoring by wearable devices
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