Investigating the Central Sensitisation Inventory (CSI). Re-establishing clinically significant values to identify central sensitization.
Recruiting
- Conditions
- chronic pain, central sensitization, pain rehabilitation, pelvic pain, back pain.
- Registration Number
- NL-OMON27116
- Lead Sponsor
- niversity Medical Center Groningen
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 1650
Inclusion Criteria
Patients:
- Patients who visited the UMCG pain center between November 1, 2017 and October 1, 2021
Healthy volunteers
- Self-reported healthy and pain-free
Exclusion Criteria
Age younger than 18 years
Healthy volunteers:
- using pain medication
- undergoing treatment for pain
- reporting a CSS diagnosis in the CSI part B
- reporting the use of antidepressants at moment of completing questionnaire
- reporting the use of anti-epileptics at the moment of completing questionnaire
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Central Sensitization Inventory
- Secondary Outcome Measures
Name Time Method