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Recruiting NCT05780021

Motivational Support Program in Chronic Low Back Pain After Multidisciplinary Functional Rehabilitation

Trial Parameters

Condition Chronic Low-back Pain
Sponsor Assistance Publique - Hôpitaux de Paris
Study Type INTERVENTIONAL
Phase N/A
Enrollment 150
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2023-09-26
Completion 2025-09-26
Interventions
Motivational Support Program Emotiv

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * age 18 or over * Disabling chronic low back pain: chronic painful patient, that is to say suffering from pain for more than 3 months, having interrupted all physical activity because of low back pain and have an indication for a FRP for low back pain. * Having reached the end of an FRP program * Possession of a smartphone * Fluency in French (writing, reading) * Health insurance coverage (beneficiary or beneficiary) except State Medical Aid. * Patient Informed Consent Signature Exclusion Criteria: * Pregnant woman * Patient refusal * Patient deprived of liberty and patient under legal protection measure (guardianship, guardianship) * Patient participating to another interventional search

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