on-inferiority of a hybrid outpatient rehabilitation due to musculoskeletal disorders: a randomized controlled trial

Not Applicable

• Conditions: M50-M54; Other dorsopathies

• Registration Number: DRKS00028770
• Lead Sponsor: niversität zu Lübeck

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-04-05
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 284

Inclusion Criteria

Rehabilitants with back pain are included (ICD-10 M50 to M54, ongoing treatment and subsequent treatment).

Exclusion Criteria

Rehabilitants without a stable internet connection, without an appropriate electronic device for playing internet browser or app-related videos and without a suitable camera for communication purposes as well as a lack of German language skills are excluded.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is pain self-efficacy, which is measured by the FESS (Fragebogen zur Erfassung der schmerzspezifischen Selbstwirksamkeit) questionnaire, the German adaption of the Pain Self-Efficacy Questionnaire (PSEQ). A total score is calculated, with a higher value representing a greater degree of pain self-efficacy (range 10–60) (Mangels et al., 2009). It is measured at all four measurement time points: start of rehabilitation (T1), end of rehabilitation (T2), 3 months after the end of rehabilitation (T3) and 12 months after the end of rehabilitation (T4).