Effect of Three Therapeutics Strategies on Patients With a Chronic Back Pain (PLURICLEF).

Phase 4UnknownNCT02030171

University Hospital, Angers158 enrolled

Overview

Effect of three therapeutics strategies on the restriction of the participation of patients with a chronic back pain : multidisciplinary is it the key component ?

Compare the efficacy of 1 year of participation, of three programs of care for patients with chronic law back, referred to specialists rehabilitation centers or directly to the multidisciplinary consultation of university hospital of Angers. The primary objectif is to assess the efficacy of 1 year of the three therapeutics strategies with the number of days off work in the year following treatment.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

158

Conditions

Chronic Low Back Pain

Interventions

functionnal reeducationOTHER

Specific functionnal reeducation for chronic low back pain

Eligibility

Sex: ALLMin age: 18 YearsMax age: 55 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Obtaining the signature of consent to participate in the study. * Male or female, aged 18-55 years. * Diagnosis of common chronic low back pain. * Chronic low back pain that led to at least a month off work in the previous year or at least 3 months of stops in the previous 2 years. * Employee and holds a permanent contract or a fixed-term contract in the public or private sector. Exclusion Criteria: * Lack of consent to participate in the study. * No possibily to follow one of three programs of study * Pregnant women, new mothers or mothers who are breastfeeding. * No affiliation to the french social system.

Locations (1)

University Hospital of Angers, laboratory epidemiology, ergonomics and occupational health

Angers, Pays de Loire, France

Outcomes

Primary Outcomes

Efficiency of the 3 programs

Compare the efficacy of 1 year of participation of the three programs of care for chronic low back pain patients referred to specialists rehabilitation centers or directly to the multidisciplinary consultation UH Angers. The primary endpoint to assess the efficacy of 1 year of support on the participation of the patient is the number of days off work in the year following treatment.

Time frame: One year

Secondary Outcomes

Evolution of quality of life scales

The secondary endpoints to assess the efficacy of 1-year quality of life of the patient is the SF-36 score. The quality of life questionnaire is collected early in the program at the end (after the 5-week program ended) at 6 months and one year.

Time frame: One year

Compare the effectiveness of 1 year on improving the social integration of three programs supported in the same patients.

The secondary endpoint to assess the efficacy of 1 year of support on improving social inclusion is the score of Dallas. The Dallas questionnaire is collected early in the program at the end (after the 5-week program ended) at 6 months and one year.

Time frame: One year

Compare the effectiveness of 1 year on physical deconditioning, three programs of care in these patients.

The secondary endpoints to assess efficacy at 1 year of support on the physical deconditioning of the patient are the finger-floor distance, Ito test, and the test port heavy load. These tests are performed early in the program at the end (after the program ended five weeks) at 6 months and one year.

Time frame: One year

Compare the cost of 1 year from the point of view of health insurance, of the three therapeutic strategies.

The secondary endpoints to assess the cost of 1 year from the point of view of health insurance, are the direct and indirect costs.

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.