Prevention of surgery-related persistent pain via the introduction of a perioperative Transitional Pain Service
Not Applicable
- Conditions
- chronic postoperative pain (ICD-11: MG 30.21)
- Registration Number
- DRKS00025799
- Lead Sponsor
- Deutsche Schmerzgesellschaft e.V.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 1860
Inclusion Criteria
Adult patients with elective surgery indication and planned inpatient stay of at least 2 days; patients who are proficient enough in the German language to understand and answer the questionnaires used
Exclusion Criteria
Patients undergoing emergency surgery; patients scheduled for outpatient surgery or whose inpatient stay is expected to be less than 48 hours; age of patient: < 18 years; patients unable to give consent; patients with insufficient knowledge of German to understand and answer the questionnaires used; pregnant patients; patients with private health insurance
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome parameters of the RCT: <br>Pain intensity index (numeric rating scales, Von Korff); pain-related functional impairment (numeric rating scales, Von Korff); physical activity (EHIS-PAQ (European Health Interview Survey - Physical Activity Questionnaire); general self-efficacy (General Self-Efficacy Expectancy (SWE) scale)
- Secondary Outcome Measures
Name Time Method