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Efficacy of the BFR-M8040 on Work-Related Neck-Shoulder Muscle Pain in Office Workers

Efficacy of the BFR-M8040 on Work-Related Neck-Shoulder Muscle Pain in Office Workers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007340
Enrollment
60
Registered
2022-06-02
Start date
2022-05-09
Completion date
Unknown
Last updated
2023-05-30

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

Conditions

None listed

Interventions

Medical Device : The control group will receive conventional physical therapy consisting of microwave and infrared radiation. The experimental group will receive the standard treatment + PEMF Neck Mod

Sponsors

Kyung Hee University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Subjects (Office workers) who meet the following criteria: (1) Complaining of non-specific muscle pain or discomfort in the neck and shoulder area for more than 3 months (2) Intensively operate keyboard or mouse for more than 4 hours a day (3) Repeat the same movement using the neck, shoulder, elbow, wrist or hands for more than 2 hours a day (4) Over 4 of NRS (Numeric Rating Scale) 2) Subjects who have agreed not to take any medication or treatments to relieve discomfort in the neck and shoulder due to work during the study period 3) Subjects who voluntarily consented, after listing enough explanation for this study and investigational device

Exclusion criteria

Exclusion criteria: 1) In the case of taking medication and related treatment to relieve muscle pain or discomfort in the neck or shoulder due within the period from screening to registration 2) have a history of surgery or trauma within the last 6 months 3) Where electronic medical devices such as implantable pacemakers are attached to or inserted into the body; 4) Where there are other skin diseases such as infectious diseases 5) Have a risk of thrombosis, embolism, or hemorrhagic 6) Where there is a severe neurological or internal disease, such as cardiovascular disease 7) Have a history of psychiatric disorders or uncontrolled epilepsy 8) Have severe osteoporosis or are currently taking medication for osteoporosis 9) Currently pregnant or have a history of childbirth within the past 6 months 10) Other cases -- when the medical staff expresses that is not suitable to participate in the study 11) Currently participating in other clinical trials for the last three months

Design outcomes

Primary

MeasureTime frame
Analyze the average change in NRS. Descriptive statistics are presented for NRS, meaning test for differences between groups using independent two-sample t-test or Wilcoxon rank-sum test, and significance test for variation within the group using paired t-test or Wilcoxon signed-rank test. When comparing the ratio differences that distinguish the operational categories between groups, the significance is tested using the Chi-square test or Fisher's exact test.

Secondary

MeasureTime frame
NRS, PPT, NDI, ROM, Korean stress measuring tool, EQ-5D-5L;Amount of change in NRS, PPT, NDI, ROM

Countries

Korea, Republic of

Contacts

Public ContactSeung-Ryong Yeom

Wonkwang University, Gwangju Medical Center

windy2589@hanmail.net+82-62-670-6461

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026