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Recruiting NCT06030570

Effect of an Interdisciplinary Spine Rehabilitation Program

— Observational Low Back Pain Spine Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Rehabilitation program (Revita).
Who it may be relevant to
Registry conditions: Low Back Pain, Spine Disease. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Belgium
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

PROGRESS: The Effect of an Interdisciplinary Program for Rehabilitation for Spinal Disorders

Overview

The goal of this research project is to evaluate the effectiveness of the current interdisciplinary rehabilitation program (Revita) and follow-up trajectory for chronic lumbar spine disorders in the University Hospitals Leuven.

Interventions

  • Other Rehabilitation program (Revita)
    Multidisciplinary programs in an outpatient hospital setting are coordinated by specialists in Physical and Rehabilitation Medicine. These programs combine a physical part (e.g., specific exercises, manual techniques) with at least one other element (psychological, social, educational or occupational intervention). In a multidisciplinary spine rehabilitation program, a maximum of 36 sessions over a maximum time period of 6 months is offered. Afterwards, a (monodisciplinary) follow-up trajectory

Primary outcome measures

  • Change in Oswestry Disability Index (ODI) [Time frame: baseline - 6 months - 1 year]
  • Change in pain [Time frame: baseline - 6 months - 1 year]
Secondary outcome measures (11)
  • Effect on quality of life [Time frame: baseline - 6 months - 1 year]
  • Effect on risk stratification tool [Time frame: baseline - 6 months - 1 year]
  • Effect on anxiety and depression [Time frame: baseline - 6 months - 1 year]
  • Effect on kinesiophobia [Time frame: baseline - 6 months - 1 year]
  • Effect on fear-avoidance beliefs [Time frame: baseline - 6 months - 1 year]
  • Effect on body awareness [Time frame: baseline - 6 months - 1 year]
  • Treatment experience [Time frame: 6 months - 1 year]
  • Return to Work self-efficacy [Time frame: baseline - 6 months - 1 year]
  • Return to work [Time frame: baseline - 6 months - 1 year]
  • Effect on functioning [Time frame: baseline - 6 months - 1 year]
  • Effect on medication use [Time frame: baseline - 6 months - 1 year]

Eligibility criteria

Inclusion criteria

  • Adults, age > 18 years
  • Spine problem for > 6 weeks, needing interdisciplinary care (risk factors, failure of first line treatment, etc)
  • Inclusion in Revita program
  • Informed consent to participate

Exclusion criteria

  • Patients without sufficient understanding of the Dutch language
  • Unable to participate in 2h rehabilitation sessions with exercises

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Belgium · 1 center
  • University Hospitals Leuven — Leuven

Identifiers

NCT: NCT06030570 · S67679

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗