M51.1
Conditions
Interventions
Group 1: Prospective randomized controlled trial (3 arms: outpatient control, post-inpatient control, intervention group).
Intervention 1:
Patients are admitted for a 7-day inpatient multimodal pain
Sponsors
Kommunalunternehmen Klinikum Fichtelgebirge
Eligibility
Sex/Gender
All
Age
18 Years to 67 Years
Inclusion criteria
Inclusion criteria: Specific low back pain with radicular symptoms lasting more than 2 weeks; pain intensity > 4 on the Numerical Rating Scale (NRS)
Exclusion criteria
Exclusion criteria: Previous surgery in the lumbar spine region, pain duration 8 weeks, patients with permanent work disability, underlying psychiatric disorders, paresis with muscle strength < 3/5 according to Janda.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain reduction (mean value NRS back and NRS leg) | — |
Secondary
| Measure | Time frame |
|---|---|
| ODI, RM, return to work (days), DASS, number of physician contacts, number of painkiller intakes, patient-centered outcomes (Patient-Reported Outcome Measures, PROMs), and patient satisfaction (Patient-Reported Experience Measures, PREMs). Process evaluation; outcomes of the health economic evaluation: disease-related costs, cost-effectiveness ratio, and incremental cost-effectiveness ratio between the groups. | — |
Countries
Germany
Contacts
Public ContactLeonie Sundmacher
Lehrstuhl für Gesundheitsökonomie
Outcome results
None listed