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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04971616
Enrollment
300
Registered
2021-07-21
Start date
2020-08-01
Completion date
2023-08-01
Last updated
2021-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain, Neck Pain, Shoulder Pain

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.

Interventions

OTHERDemographic data and range of motion.

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.

Sponsors

Peking University Third Hospital
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* 20-40 year of age with symptoms of shoulder * Neck and lower back discomfort

Exclusion criteria

* Red flag sign of the neck

Design outcomes

Primary

MeasureTime frameDescription
Range of motion (ROM) of the neckat least 2-week monitoring by wearable devicesPatients' range of motion of the neck in all directions are measured using hand-held devices.
Oswestry Disability Index (ODI)at least 2-week monitoring by wearable devicesOswestry Disability Index of the neck is collected for the evaluation of neck functions.
Visual Analogue Scale (VAS)at least 2-week monitoring by wearable devicesVisual Analogue Scale is collected for pain assessment.
Roland-Morris Disability Questionnaire (RDQ)at least 2-week monitoring by wearable devicesRoland-Morris Disability Questionnaire is collected for the evaluation of lower back functions.

Countries

China

Contacts

Primary ContactJian-quan Wang, M.D.
keny1417@vip.sina.com13801076267

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026