Actively Recruiting
Motivational Support Program in Chronic Low Back Pain After Multidisciplinary Functional Rehabilitation
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-08-22
150
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Chronic low back pain (CLBP) is a major public health problem. Multidisciplinary functional rehabilitation program (FRP), which give patients the skills to better manage pain and return to physical activity, are effective in the short term. In the medium and long term, due to lack of motivation, two thirds of patients stop their physical activity again, causing them to fall back into the vicious circle of pain. Investigators hypothesise that a remote assessment and motivational support program (MSP) based on an application, piloted by a care coordinator, could allow the continued improvement of symptoms and activities observed after the FRP programs, and thus limit the consequences of CLBP for the patient and society. The main objective of this study is to evaluate the effect of the motivational support program EMOTIV, on disability and pain at one year, in chronic low back pain patients who have benefited from a FRP program.
CONDITIONS
Official Title
Motivational Support Program in Chronic Low Back Pain After Multidisciplinary Functional Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Chronic disabling low back pain lasting more than 3 months
- Interrupted all physical activity due to low back pain
- Completed a multidisciplinary functional rehabilitation program
- Own a smartphone
- Able to read and write in French
- Have health insurance coverage (excluding State Medical Aid)
- Provided signed informed consent
You will not qualify if you...
- Pregnant women
- Patients who refuse to participate
- Patients deprived of liberty or under legal protection measures (such as guardianship)
- Patients currently participating in another interventional study
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hôpital Pitié Salpêtrière
Paris, France, 75013
Actively Recruiting
Research Team
V
Violaine FOLTZ, Dr
CONTACT
B
Bruno FAUTREL, Pr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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