Different trajectories for people with acute neck pain: associations with biological, psychosocial and treatment-related factors.
- Conditions
- acute painNeck pain10023213
- Registration Number
- NL-OMON49410
- Lead Sponsor
- Vrije Universiteit
- Brief Summary
Trial is onging in other countries
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
People with non-specific neck pain will be eligible for participation if they
are: 1) at least 18 years old, 2) within 2 weeks of onset of an acute neck pain
episode, 3) lasting for >24h, and 4) having sufficient knowledge of the Dutch
language.
* Pregnancy or postpartum for not more than 9 months or those who give
breastfeeding;
* Contra-indications for venipuncture;
* Taking one of the following medications during the last 6 weeks:
corticosteroids (e.g. prednisone), immunomodulatory medication (e.g.
methotrexate, infliximab) and the use of botox for the last 3 months;
* Current participation in another clinical trial;
* Having a medical disease with immune system involvement (e.g. MS, Spondylitis
Ankylpoetica).
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method