Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT07051772

Predictive Factors for the Success of Rehabilitation Programs in Chronic Low Back Pain

Led by Centre Hospitalier Universitaire de Nīmes · Updated on 2026-01-16

333

Participants Needed

6

Research Sites

179 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic low back pain is the leading cause of years lived with disability in the world among 19-49 year olds. The usual progression leads to 15% of acute episodes of persistent pain and more than 50% of persistent activity limitations. Persistent pain lasting between 5 and 7 years causes relatively stable patterns, probably linked to well-known predictive factors of activity limitations such as psychosocial factors (catastrophizing, fears and maladaptive beliefs), physical (deconditioning), professional (fear of returning to work, stress, burden) or personal (financial, insecurity). The effectiveness of treatments is often difficult to predict. Current evidence does not support the use of pharmacological treatments given their low effectiveness and the risks associated with the prescription of non-steroidal anti-inflammatories or opioids, particularly in the chronic phase where the risk of dependence is highest. Thus, international recommendations strongly suggest the use of non-pharmacological therapies, including, physical exercises, rehabilitation, physical and sports activities and spinal manipulations. Most meta-analyses conclude that there is a cumulative effect of the different strategies, without the specific effect of each one being able to be isolated, justifying multidisciplinary protocols. A cornerstone of the management of chronic disabling low back pain therefore relies programs combining physical, cognitive-behavioral, psychological and professional care, most often in dedicated centers. The objective is to empower the patient and promote a change in behavior with regard to the consequences of their pain in the long-term. However, there are very few predictive criteria for the success or failure of these programs, probably because many multiple biological, psychological, and social factors interact over time. Certain models resulting from expert consensus seek to conceptualize these interactions and propose a categorization of these different factors. It is now crucial to validate these categorizations and their relative weight in the progression of patients to best guide their recovery. The aim of this work is to identify the biomarkers predictive of the success of multidisciplinary programs in the short-, medium- and long-term.

CONDITIONS

Official Title

Predictive Factors for the Success of Rehabilitation Programs in Chronic Low Back Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with chronic low back pain lasting three months or more
  • Patient has given free and informed consent and signed the consent form
  • Patient is a member or beneficiary of a health insurance plan
Not Eligible

You will not qualify if you...

  • Patient is participating in a category 1 interventional study or a medication/device study without approval from the primary investigator
  • Patient is currently in an exclusion period from a previous study
  • It is impossible to provide the patient with informed information
  • Patient is under legal protection such as safeguard of justice or state guardianship
  • Patient is treated for psychiatric, cancerous, or orthopedic conditions that may affect care
  • Patient is pregnant, giving birth, or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 6 locations

1

CHU de Clermont Ferrand

Clermont-Ferrand, Auvergne, France, 63000

Not Yet Recruiting

2

Centre Hospitalier Universitaire de Nîmes

Nîmes, Gard, France, 30900

Not Yet Recruiting

3

CHU de Montpellier

Montpellier, Occitanie, France, 34000

Not Yet Recruiting

4

CHU de Nîmes

Nîmes, Occitanie, France, 30029

Actively Recruiting

5

CHU de Clermont-Ferrand

Clermont-Ferrand, France

Not Yet Recruiting

6

CHU de Montpellier

Montpellier, France

Not Yet Recruiting

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Research Team

A

Arnaud Dupeyron

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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