This site became the new on June 19th. Learn more.
Show more Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu
Give us feedback

Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified October 2010 by Hillel Yaffe Medical Center.
Recruitment status was:  Not yet recruiting
Headway Ltd.
Information provided by:
Hillel Yaffe Medical Center Identifier:
First received: June 1, 2010
Last updated: October 6, 2010
Last verified: October 2010
The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.

Condition Intervention Phase
Neck Pain Device: Occiflex Device Phase 1 Phase 2

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment

Resource links provided by NLM:

Further study details as provided by Hillel Yaffe Medical Center:

Primary Outcome Measures:
  • Safety of computerized continuous mobilization of the cervical spine [ Time Frame: one year ]

Secondary Outcome Measures:
  • Efficacy of computerized mobilization of treatment of patients with chronic neck pain [ Time Frame: one year ]

Estimated Enrollment: 10
Study Start Date: December 2010
Estimated Study Completion Date: May 2011
Estimated Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: I. Patients with chronic neck pain Device: Occiflex Device
This device is a computerized robotic platform that allows continuous mobilization of the cervical spine in a three dimensional space. The patients undergoes biweekly 20 minute therapeutic session for 6 weeks


Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01216566

Hillel Yaffe Medical Center Not yet recruiting
Hadera, Israel, 38100
Contact: Yaron M River, MD    972-4-6304427   
Sub-Investigator: Jill Bracha, PT         
Sponsors and Collaborators
Hillel Yaffe Medical Center
Headway Ltd.
  More Information

Responsible Party: Yaron River, MD, Dept. of Neurology, Hillel Yaffe Medical Center Identifier: NCT01216566     History of Changes
Other Study ID Numbers: HYMC-0030-10
Study First Received: June 1, 2010
Last Updated: October 6, 2010

Additional relevant MeSH terms:
Neck Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms processed this record on September 19, 2017