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Comparison of manual therapy with Occiflex therapy for work-related neck disorders: a randomized controlled study

Effect of Occiflex, an intelligent bionic neck motion system, on work-related neck disorders

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053076
Enrollment
Unknown
Registered
2021-11-10
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-09-06

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

Conditions

neck pain

Interventions

A group:Therapeutic exercise + mission
B group:Occiflex + therapeutic exercise + mission
C group:Manual therapy + therapeutic exercise + mission

Sponsors

The Sixth Affiliated Hospital in Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1.Office workers aged 18 to 55 years and used computers for more than four hours a day on average; 2.The duration of neck and shoulder pain was more than 3 months, and the VAS was not less than 5; 3.Have fixed contact information and can receive long-term treatment (10 times in 4 weeks) and follow-up (3 months); 4.Volunteer to participate in research; 5.Patients who can tolerate Occiflex treatment or do not cooperate with the test.

Exclusion criteria

Exclusion criteria: 1.Headache or dizziness caused by exact pathological factors, such as cerebrovascular disease involving vertebral artery, intracranial vascular malformation, hydrocephalus, cerebral hemorrhage or secondary headache caused by cerebrovascular defect (such as cerebral hemangioma); 2.Radiographically confirmed cervical vertebra fracture, tumor, tuberculosis, and severe disc herniation pressing on the spinal cord; 3.Obvious signs of nerve damage, such as loss of sensation and weakened muscle strength; 4.Recurrent dizziness or dizziness; 5.Cognitive impairment.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale for pain;Neck pain dysfunction questionnaire;

Secondary

MeasureTime frame
Improvement of neck motion;The tenderness threshold of C2 spinous process and midpoint of bilateral trapezius muscle;Adverse reactions;Self overall feeling recovery after treatment;

Countries

China

Contacts

Public ContactWang Yuling

The Sixth Affiliated Hospital of Sun Yat-Sen University

wangyul@mail.sysu.edu.cn+86 13054445587

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026