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Interprofessional Rehabilitation for Adults With Chronic Non-specific Low Back Pain (PASTOR)

U

University of Erlangen-Nürnberg

Status

Completed

Conditions

Low Back Pain

Treatments

Procedure: Interprofessional rehabilitation
Procedure: Multidisciplinary rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT02056951
0421-FSCP-0529

Details and patient eligibility

About

The primary aim of the study is to analyse the long-term effectiveness of an interprofessional and interdisciplinary rehabilitation program named "PASTOR", with a biopsychosocial approach for participants with chronic non-specific low back pain (CLBP) compared to the standard inpatient multidisciplinary orthopaedic rehabilitation (MOR) in Germany. The investigators hypothesize that in adults with CLBP the rehabilitation program PASTOR would result in a significantly higher increase in functional ability 12 months after completion of the program in comparison to the standard inpatient MOR. The investigators further hypothesize that PASTOR would lead to significantly larger improvements regarding pain-related cognitions, pain coping strategies, physical activity, health-related quality of life, and back pain episodes compared to the standard inpatient MOR.

Enrollment

536 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • M51.2 Other specified intervertebral disc displacement
  • M51.3 Other specified intervertebral disc degeneration
  • M51.4 Schmorl's nodes
  • M51.8 Other specified intervertebral disc disorders
  • M51.9 Intervertebral disc disorder, unspecified
  • M53.8 Other specified dorsopathies
  • M53.9 dorsopathy, unspecified
  • M54.4 Lumbago with sciatica
  • M54.5 Low back pain
  • M54.6 Pain in thoracic spine
  • M54.8 Other dorsalgia
  • M54.9 Dorsalgia, unspecified

Exclusion criteria

  • age below 18 years or over 65 years
  • specific underlying diagnosis of back pain (e. g. radicular symptoms, myelopathy)
  • considerably reduced health status (e.g. comorbidity)
  • considerably reduced sight and hearing (not corrected)
  • severe psychiatric condition as secondary diagnosis
  • inability to speak German
  • current application for early retirement or invalidity pension (§51 SG V - german law)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

536 participants in 2 patient groups

Multidisciplinary rehabilitation
Active Comparator group
Description:
The central objective of inpatient multidisciplinary orthopedic rehabilitation (MOR) is to improve functional health with the main focus on restoring and improving work ability. A MOR lasts on average 23 days with a total extent of therapy of 48 hours on average. MOR is provided by a multiprofessional team consisting of physicians, psychologists, sport therapists, physiotherapists, occupational therapists, masseurs, social workers, dieticians and nurses. The interventions are carried out mainly in open groups.
Treatment:
Procedure: Multidisciplinary rehabilitation
Interprofessional rehabilitation
Experimental group
Description:
The central objective of the interprofessional rehabilitation (PASTOR) is the development of active self-management of chronic non-specific low back pain. PASTOR is matched to the MOR with respect to the total duration and total extent of therapy, the included professions and the interventions dimensions (physical, psychological). The differences between PASTOR and MOR are characterized by, a) an integrative combination of profession related modules within a comprehensive and consistent treatment approach, b) an interprofessional and collaborative teamwork based on profession related modules, c) the use of standardized methods, media and materials by all professions in the therapeutic team d) a highly structured and detailed manual for the entire treatment process. The interventions are carried in fixed groups with eight to twelve participants.
Treatment:
Procedure: Interprofessional rehabilitation

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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