Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Motor imagery to improve function in adults with chronic low back pain

Official title: Impact of Motor Imagery in the Functional Rehabilitation of Patients With Chronic Low Back Pain: a Randomised Controlled Trial

Run by Centre Hospitalier Universitaire Dijon · NCT07111286 · Data updated 2026-11-12

This study tests whether guided motor imagery sessions can help adults with chronic non-specific low back pain reduce fear of movement and improve daily function.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment72 (estimated)
SponsorCentre Hospitalier Universitaire Dijon
Academic / other
Locations1 site (Dijon)
StatusRecruiting
StartedJanuary 22, 2026
Main results expectedMarch 2028
Study endsMarch 2028
Registry record updatedJanuary 27, 2026
Trial IDNCT07111286 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with chronic non-specific low back pain lasting more than six months who are eligible for a multimodal rehabilitation program and can give informed consent.

Probably not a fit

People with radicular pain with significant motor deficit, major non-spinal conditions that limit mobility, planned lumbar surgery within a year, pregnancy, or inability to consent are unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a randomized controlled trial at CHU Dijon Bourgogne comparing repeated motor imagery task sessions to control cognitive task sessions as part of a multimodal rehabilitation pathway for chronic non-specific low back pain. Participants receive baseline and follow-up clinical assessments, ongoing motor imagery or cognitive tasks, and evaluations of satisfaction and tolerance. Primary outcomes focus on functional ability, kinesiophobia, and patient-reported pain and quality of life measures. The protocol excludes patients with major neurologic or orthopedic conditions, significant mobility-limiting comorbidities, planned lumbar surgery, or inability to consent.

Why it matters

Potential benefit: If successful, motor imagery could reduce fear-related avoidance and help patients regain daily and professional activities with less pain-related limitation.

How similar studies have gone: Motor imagery has shown promise in small studies for stroke and some chronic pain conditions, but evidence specifically for chronic low back pain is limited and mixed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patient
* Person who has given their verbal consent
* Suffering from chronic non-specific low back pain that has been ongoing for more than 6 months
* Eligible for a multimodal rehabilitation programme according to the investigating physician

Exclusion Criteria:

* Persons not affiliated with or not covered by a social security scheme
* Patients subject to legal protection measures (guardianship, curatorship)
* Patients subject to judicial protection measures
* Pregnant women, women in labour or breastfeeding women
* Adults who are incapacitated or unable to give their consent
* Patients with a history of repeated falls
* Scheduled lumbar spine surgery in the coming year
* Associated conditions other than spinal conditions (orthopaedic, neurological, vascular, cardiac, etc.) that could significantly impair mobility
* Radicular involvement (sciatica or cruralgia) with motor deficit \< 3 in the lower limbs
* Impaired comprehension skills making self-assessment impossible
* Patients with poorly controlled epilepsy
* Individuals who are not fluent in English
* Patients who have already completed a multimodal rehabilitation programme in a specialised centre

Where it's running

  • CHU Dijon Bourgogne
    Dijon, France
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.