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Clinical Trials/NCT05261828
NCT05261828CompletedNot 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 enrollmentStarted: February 14, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
100
Locations
1
Primary Endpoint
low back pain activity limitation

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.
  • •Patients having followed a multidisciplinary rehabilitation program for their low back pain in the 3 months preceding inclusion.
  • •Patients who have had lumbar spine surgery within the last 12 months.
  • •Pregnancy in progress.
  • •No affiliation with a health insurance program.

Arms & Interventions

A

Experimental

Short multidisciplinary program including education and rehabilitation and a personalized follow-up program

Intervention: Education and rehabilitation associated with personalized follow-up (Behavioral)

B

Active Comparator

Reassuring messages and advices in agreement with the current recommendations.

Intervention: Reassuring messages and advices (Behavioral)

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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