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Clinical Trials/NCT05261828
NCT05261828
Completed
Not Applicable

Efficacy of a Short Multidisciplinary Education and Rehabilitation Program for Patients With Subacute and Chronic Low Back Pain (LBP)

Assistance Publique - Hôpitaux de Paris1 site in 1 country100 target enrollmentFebruary 14, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non Specific Low Back Pain
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
100
Locations
1
Primary Endpoint
low back pain activity limitation
Status
Completed
Last Updated
5 months ago

Overview

Brief Summary

The main purpose of this study is to assess the clinical efficiency of an intervention including a short multidisciplinary program of education and rehabilitation and a personalized follow-up, in patients with subacute and chronic low back pain and no severe disability. The secondary objectives are:

  • to assess the capacity of the program to modify and reduce the risk factors for evolution of patients towards a severe disability,
  • to estimate the cost-utility ratio of the intervention.

Detailed Description

Non-specific low back pain (LBP) is the leading cause of years lived with disability worldwide. Subacute LBP is commonly defined as back pain lasting between 6 weeks and 3 months, chronic LBP as pain that persists for 3 or more months. In its most severe forms, subacute and chronic LBP can lead to severe disability that combines physical and psychological deconditioning, limitations in basic and complex activities of daily living, professional exclusion and social marginalization. The direct and indirect medical and economic cost of chronic LBP is major for society. Since the eighties, the bio-psycho-social approach has emerged for the treatment of people with chronic LBP and has led to multidisciplinary functional restoration (FR) programs that include physical activity, exercises, education, occupational therapy and psychological and social rehabilitation. However, the efficiency of these programs is inconsistent and their cost-effectiveness is criticized. As FR programs are by definition standardized, the treatment of chronic LBP remains poorly stratified. However, interest in stratified therapeutic strategies has recently emerged and shown promising results. To date, in France, only semi-intensive (\<100h) or intensive (\>100h) FR programs dedicated to severely disabled patients with chronic LBP have been assessed The investigators' main hypothesis is that an intervention consisting in a short multidisciplinary program including education and rehabilitation and a personalized follow-up could reduce the activity limitations of not severely disabled patients with subacute and chronic LBP. The investigators' secondary hypothesis is that such an intervention could also reduce the main risk factors for evolution of patients with LBP towards a severe disability.

Registry
clinicaltrials.gov
Start Date
February 14, 2023
End Date
November 10, 2025
Last Updated
5 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with subacute or chronic nonspecific low back pain (current episode duration ≥ 6 weeks), resistant to outpatient management, and including patients with radiculopathy as long as low back pain is predominant over pain in the lower extremity.
  • Patients with less than 30 days off work (declarative) for low back pain in the previous year and involved in a professional activity at the time of inclusion.
  • Patients manifesting fears and false beliefs and/or dramatization: to be included, the patient will have to answer yes to one of the following two questions:
  • Are you afraid to move?
  • Are you afraid you will never get out of it?
  • Patients eligible for a rehabilitation exercise program
  • informed and written consent to participate
  • Exclusion Criteria
  • Age \< 18 years,
  • Insufficient French language proficiency.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

low back pain activity limitation

Time Frame: 3 months

Variation in the level of low back pain- activity limitation assessed by the Roland-Morris self-administered questionnaire (0, no limitation and 24, maximum limitation)

Secondary Outcomes

  • fears and beliefs about work(3 months)
  • radicular pain(3 months)
  • low back pain activity limitation(6 and 12 months.)
  • low back pain(3 months)
  • fears and beliefs about physical activity(3 months)
  • days off work(3 and 12 months)
  • cost-utility ratio(12 months)

Study Sites (1)

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