Skip to content

Sensorimotor Neck Study, towards an Objective Approach of non-specific neck pain.

Sensorimotor Neck Study, towards an Objective Approach of non-specific neck pain. - Sensorimotor Neck Study (SNS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38322
Enrollment
120
Registered
2012-10-16
Start date
2012-11-02
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Stoornissen van het houdings en bewegingsapparaat. neckpain Non traumatic neckpain

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Subjects are included if the they have non specific neck pain not longer then a year uninterrupted. Only adults (both males and females) under 60 years of age will be included. Subjects should be physically able to undergo COR, VOR and OKR measurements (sitting in a chair for 30 min; biting on a bite-board; staying comfortabel in a dark room). Vision should be good enough to be able to trace a laser dot on a dark background without glasses. Likewise, they should be able of understanding and filling in the questionnaire and giving informed consent. The subjects within the control group should have no complaints of the cervical spine at all. All subjects should have no history of a car accident.

Exclusion criteria

Exclusion criteria: Subjects should not use medication that influences alertness or balance (e.g. benzodiazepines, barbiturates), they should not suffer from any neurological disorder and have no vestibular problems. All subjects with a history of a neck trauma including due to a car accident are excluded.

Design outcomes

Primary

MeasureTime frame
The main research variables are the gain (ratio between eye and stimulus movement) of the COR, VOR and OKR. The degree of smooth pursuit of the eye in tracking a moving laser dot. The level of joint position error The difference in active movement of the upper cervical spine (C0-C3) and the mid cervical spine (C3-C7).

Secondary

MeasureTime frame
The secondary outcomes are the active ROM of the cervical spine, the perceived pain and the perceived functioning of the cervical spine.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)