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

Status

UNKNOWN

Phases

Phase 1Phase 2

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01216566

Enrollment

Registered

2010-10-07

Start date

2010-12-31

Completion date

2011-05-31

Last updated

2010-10-07

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

Conditions

Neck Pain

Brief summary

The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.

Interventions

DEVICEOcciflex 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

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Safety of computerized continuous mobilization of the cervical spine	one year

Secondary

Measure	Time frame
Efficacy of computerized mobilization of treatment of patients with chronic neck pain	one year

Countries

Israel

Outcome results

None listed

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