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

NCT ID: NCT05840302

Last Updated: 2025-09-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

82 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-02

Study Completion Date

2027-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Low Back Pain, Recurrent

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Pain Neuroscience Education

The Pain Neuroscience Education program takes place over ten days consisting of providing knowledge about the neurophysiology and central processes of pain (nociceptive pathways, inhibitory circuits, peripheral and central sensitization, nervous system plasticity) as well as psychosocial factors and beliefs contributing to chronic pain. Workshops will use experimental data from neuroscience, but also analogies, brainstorming or games. Questions are proposed to the patient at the end of each theme.

Group Type EXPERIMENTAL

Activity monitor

Intervention Type DEVICE

Measure of number of steps and physical activity during one week using the activity monitor (connected watch) named the ActiGraph-wGT3X-BT medical device, Pre-test before intervention, post-test 3-months and 1-year after intervention

Questionnaire

Intervention Type OTHER

Self and hetero assessments measuring pain, different determinants of chronic pain and physical activity

Back School

The Back School program takes place over ten days. It begins with a presentation of spinal economy, which consists of promoting the protection of the back. Then, the anatomy and biomechanics of the spine as well as the most common spinal pathologies are presented. On this biomechanical basis, the other sessions consist in indicating the gestures and postures to adopt, always according to the protection policy, in different situations. These different sessions alternate between theory and practical exercises.

Group Type ACTIVE_COMPARATOR

Activity monitor

Intervention Type DEVICE

Measure of number of steps and physical activity during one week using the activity monitor (connected watch) named the ActiGraph-wGT3X-BT medical device, Pre-test before intervention, post-test 3-months and 1-year after intervention

Questionnaire

Intervention Type OTHER

Self and hetero assessments measuring pain, different determinants of chronic pain and physical activity

Interventions

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Activity monitor

Measure of number of steps and physical activity during one week using the activity monitor (connected watch) named the ActiGraph-wGT3X-BT medical device, Pre-test before intervention, post-test 3-months and 1-year after intervention

Intervention Type DEVICE

Questionnaire

Self and hetero assessments measuring pain, different determinants of chronic pain and physical activity

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient over 18 years of age.
* Ordinary back pain according to the High Authority for Health criteria 2019
* Chronic back pain (\> 3months)
* Start Back Screening Tool \> 3
* Partial hospitalization at the Lamalou-les-Bains Hospital for a multidisciplinary rehabilitation program

Exclusion Criteria

* Subject with a comorbidity that limits walking (e.g. central neurological disorder)
* Subject with current psychiatric or cognitive co-morbidity that does not allow educational programs to be completed
* Stay following a surgical procedure of less than three months
* Other specific low back pain treatment planned during the 3 months of follow-up (surgery, infiltration)
* Patient participating in another clinical trial related to low back pain
* Subject does not understand the French language.
* Pregnant woman, parturient or nursing
* Subject with a legal protection measure (guardianship, curators)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Montpellier

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hospital Center Paul Coste Floret

Lamalou-les-Bains, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Gaël LE PERF

Role: CONTACT

0467235729 ext. +33

Guillaume THEBAULT

Role: CONTACT

0467235511 ext. +33

Facility Contacts

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Gaël LE PERF

Role: primary

0467235729

Guillaume THEBAULT

Role: backup

0467235511

References

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Thebault G, Duflos C, Le Perf G. Effectiveness of a pain neuroscience education programme on the physical activity of patients with chronic low back pain compared with a standard back school programme: protocol for a randomised controlled study (END-LC). BMJ Open. 2024 Jun 3;14(6):e080079. doi: 10.1136/bmjopen-2023-080079.

Reference Type DERIVED
PMID: 38830744 (View on PubMed)

Other Identifiers

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ID-RCB

Identifier Type: REGISTRY

Identifier Source: secondary_id

RECHMPL21_0513

Identifier Type: -

Identifier Source: org_study_id

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