Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05840302

Effectiveness of a Pain Neuroscience Education Programme on Physical Activity in Patients With Chronic Low Back Pain

Led by University Hospital, Montpellier · Updated on 2025-09-30

82

Participants Needed

1

Research Sites

204 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Proposing ways to effectively counter chronic low back pain through non-drug intervention is a major public health issue due to the prevalence and health costs of this condition. The back school (BS) is based on spinal economics and a biomechanical model. A convergence of evidence indicates that this type of program does not bring any mid- or long-term benefit. Faced with this observation, a Pain Neuroscience Education (PNE) has been developed based on a biopsychosocial model. Chronic low back pain is the consequence of a complex dynamic of multifactorial origin where the body lesion is no longer the only cause of the pain. Studies have shown that PNE has a positive effect on pain perception. One of the limitations of these studies is that they do not allow objective measurement of physical activity performed at a distance from a therapeutic program for patients who have benefited from these educational programs. Yet, physical activity is an essential variable in health and more specifically in the fight against pain in patients with chronic low back pain. The investigators believe that physical activity is a key factor in improving the condition of patients with chronic low back pain. Consequently, physical activity is an indicator of success but also a guarantee for a lasting effect of educational treatment. In order to measure this physical activity, the use of activity monitor (connected watch) developed in recent years now makes it possible to collect data in an ecological manner that is more objective than the data collected via self-questionnaires. The main objective of the study is to measure the effectiveness of a PNE on physical activity three months after the intervention compared to BS in patients with chronic low back pain receiving a multidisciplinary rehabilitation program. The secondary aims are to compare effectiveness of PNE versus BS on pain, quality of life, kinesiophobia, pain catastrophizing, central sensitization at 3 months and at one year after the intervention. In addition, an exploratory analysis will be conducted to determine predictors of physical activity maintenance. The investigators expect to observe greater physical activity in patients who have received a PNE program compared to the physical activity of patients who have completed an BS program.

CONDITIONS

Official Title

Effectiveness of a Pain Neuroscience Education Programme on Physical Activity in Patients With Chronic Low Back Pain

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient over 18 years of age.
  • Ordinary back pain according to the High Authority for Health criteria 2019
  • Chronic back pain (more than 3 months)
  • Start Back Screening Tool score greater than 3
  • Partial hospitalization at the Lamalou-les-Bains Hospital for a multidisciplinary rehabilitation program
Not Eligible

You will not qualify if you...

  • Comorbidity that limits walking (e.g., central neurological disorder)
  • Current psychiatric or cognitive comorbidity preventing completion of educational programs
  • Less than three months since a surgical procedure
  • Planned specific low back pain treatments during 3-month follow-up (surgery, infiltration)
  • Participation in another clinical trial related to low back pain
  • Does not understand the French language
  • Pregnant, giving birth, or nursing
  • Subject under legal protection measures (guardianship, curatorship)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hospital Center Paul Coste Floret

Lamalou-les-Bains, France, 34240

Actively Recruiting

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Research Team

G

Gaël LE PERF

CONTACT

G

Guillaume THEBAULT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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