Risk Screening and Assessment of Shoulder, Neck and Lower Back Discomfort.

• Conditions: Neck Pain; Low Back Pain; Shoulder Pain
• Interventions: Other: Demographic data and range of motion.

• Registration Number: NCT04971616
• Lead Sponsor: Peking University Third Hospital

Brief Summary

Identifying high-risk factors that may lead to shoulder, neck and lower back discomfort and contributing to the primary prevention of disease progression.

Detailed Description

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 Timeline

• Study Start: 2020-08-01
• Study First Submitted: 2021-06-27
• Status Verified: 2021-07
• Study First Submitted QC: 2021-07-11
• Last Update Submitted: 2021-07-11
• Study First Posted: 2021-07-21
• Last Update Posted: 2021-07-21
• Primary Completion: 2021-08-01
• Study Completion: 2023-08-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Group 1: Patients with shoulder, neck and lower back discomfort	Demographic data and range of motion.	Patients with shoulder, neck and lower back discomfort.

Primary Outcome Measures

Name	Time	Method
Oswestry Disability Index (ODI)	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)	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	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)	at least 2-week monitoring by wearable devices	Visual Analogue Scale is collected for pain assessment.

Trial Locations

Locations (1)

Peking University Third Hospital; 🇨🇳 Beijing, China