Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain
Phase 1
- Conditions
- Neck Pain
- Registration Number
- NCT01216566
- Lead Sponsor
- Hillel Yaffe Medical Center
- Brief Summary
The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
- Patients with chronic neck pain: post-whiplash injury, myofacial pain, cervical facet joint disease and idiopathic chronic neck pain
Exclusion Criteria
- Radiculopathy
- Myelopathy
- Cerebral vascular disease
- Malignancy
- Osteoporosis
- Cervical disc herniation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Safety of computerized continuous mobilization of the cervical spine one year
- Secondary Outcome Measures
Name Time Method Efficacy of computerized mobilization of treatment of patients with chronic neck pain one year
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the Occiflex device's efficacy in treating chronic neck pain?
How does the Occiflex device compare to manual cervical mobilization in pain reduction and functional outcomes?
Are there specific biomarkers that predict response to cervical spine mobilization using the Occiflex device?
What adverse events are associated with computerized cervical spine mobilization and how are they managed?
What are the potential combination therapies for chronic neck pain alongside the Occiflex device?
Trial Locations
- Locations (1)
Hillel Yaffe Medical Center
🇮🇱Hadera, Israel
Hillel Yaffe Medical Center🇮🇱Hadera, Israel