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

A

Assistance Publique - Hôpitaux de Paris

Status

Active, not recruiting

Conditions

Non Specific Low Back Pain

Treatments

Behavioral: Education and rehabilitation associated with personalized follow-up
Behavioral: Reassuring messages and advices

Study type

Interventional

Funder types

Other

Identifiers

NCT05261828
APHP200142
2020-A02601-38 (Other Identifier)

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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.
  • 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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

A
Experimental group
Description:
Short multidisciplinary program including education and rehabilitation and a personalized follow-up program
Treatment:
Behavioral: Education and rehabilitation associated with personalized follow-up
B
Active Comparator group
Description:
Reassuring messages and advices in agreement with the current recommendations.
Treatment:
Behavioral: Reassuring messages and advices

Trial contacts and locations

1

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Central trial contact

Christelle NGUYEN, MD, PhD; Laetitia PEAUDECERF, PhD

Data sourced from clinicaltrials.gov

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