Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04826757
Other study ID # 2020-A01039-30
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 21, 2022
Est. completion date September 2026

Study information

Verified date April 2024
Source University Hospital, Angers
Contact Aline RAMOND ROQUIN, MD-PHD
Phone 0241735867
Email aline.ramond@univ-angers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Common low back pain affects about 23% of general population and can be associated with psychosocial difficulties and prolonged inability to work. Its management in France mainly depends on general practioners, and sometime on physiotherapists. A coordinated care between general practioners, physiotherapists and occupational health services would help to improve the care pathway for patients and health professionals. The main objective is to assess the impact of coordinated primary care and deployed at the territories' level, in subacute or acute recurrent low back pain patients in comparison with the standard care.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date September 2026
Est. primary completion date September 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Patient consulting an investigator GP for subacute low back pain or acute recurrent low back pain - Patient with occupational activity (including sick leave) - Patient depending of occupational health service - Obtaining the signature of the consent to participate in this trial - Patient Registered with social security scheme Non-inclusion Criteria: - Specific low back pain (fracture, infection, osteoporosis, inflammatory disease, tumor) - Low back pain with sciatic, cruralgia - Contraindication to active reeducation - Impossibility to follow up during 12 months - Patient planning to retire within the 12 months following the enrollment - Disability to write or read french - Adult patient protected under the law (guardianship), - Pregnant, breastfeeding or parturient women - Persons deprived of their liberty by judicial or administrative decision - Persons subject to legal protection measures - Persons unable to consent - Persons on coercion psychiatric care - Physiotherapy by a physiotherapist who don't participate in this trial

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Coordinated care
Coordinated care between general practioners; physiotherapists and occupational health services. Early contact with occupational health service by the general practioner and use of occupational retention tool Active physiotherapy (Individual active, intensive and regular rehabilitation program with 15 sessions of 1 hour, at a rate of 2 or 3 sessions per week)

Locations

Country Name City State
France Cluster Bonchamp Bonchamp-lès-Laval
France Cluster Vaunoise Breteil
France Cluster BRULON Brulon
France Cluster Château Gontier Château-Gontier
France Cluster Châteauneuf sur Sarthe / Morannes Châteauneuf-sur-Sarthe
France Cluster Clisson Clisson
France Cluster Conlie Conlie
France Cluster Craon Renaze Cosse Craon
France Cluster Entrammes Laval Entrammes
France Cluster Roche sur Yon La Roche-sur-Yon
France Cluster Chantenay Nantes
France Cluster Dinan / Quévert / Plouasne Quévert
France Cluster Rennes Beauregard Rennes
France Cluster Rennes Villejean Rennes
France Cluster Les Collines Roquefort les pins
France Cluster St Florent, Mauges, Possonnière Saint-Florent-le-Vieil
France Cluster Savenay Savenay
France Cluster SEGRE Segré
France Cluster Angers- Trélazé Trélazé
France Cluster Vence Vence

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived inability at 1 year Ratio of patient presenting improvement equal or above 4 points of Roland Morris Disability Questionnaire. The minimum value of Roland Morris Disability Questionnaire is 0 and the maximun value is 24. A higher score mean worse outcome Enrollment to 12 months follow up
Secondary Perceived inability Ratio of patient presenting improvement equal or above 4 points of Roland Morris Disability Questionnaire. The minimum value of Roland Morris Disability Questionnaire is 0 and the maximun value is 24. A higher score mean worse outcome Enrollment to 3 months follow up, Enrollment to 6 months follow up
Secondary Roland Morris Disability score over time Evolution of Roland Morris Disability Questionnaire over time. The minimum value is 0 and the maximun value is 24. A higher score mean worse outcome Enrollment, 3 months, 6 months, 12 months
Secondary Pain perceived Ratio of patients presenting improvement equal or above 2 points of numerical pain scale The minimum value is 0 and the maximun value is 10. A higher score mean worse outcome Enrollment - 3 months , Enrollment - 6 months and Enrollment -12 months
Secondary Numerical pain scale over time Evolution of numerical pain scale over time. The minimum value is 0 and the maximun value is 10. A higher score mean worse outcome Enrollment, 3 months, 6 months, 12 months
Secondary Occupational status Ratio of patients having an active occupation (defined by have an employment and be present at work ) at 3 months, 6 months and 12 months
Secondary Employment rate Evolution of employment rate over time Enrollment, 3 months, 6 months, 12 months
Secondary Sick leave number of sick leave days during 12 months after inclusion
Secondary Improved patients Ratio of improved patients. Improved patients is defined by patient presenting improvement equal or above 4 points of Roland Morris Disability Questionnaire and improvement equal or above 2 points of numerical pain scale and having a active occupational at 3 months, 6 months and 12 months
Secondary Evolution of improved patients ratio Evolution of improved patients ratio over time Improved patients is defined by patient presenting improvement equal or above 4 points of Roland Morris Disability Questionnaire and improvement equal or above 2 points of numerical pain scale and having a active occupational Enrollment, 3 months, 6 months, 12 months
Secondary Mental component score of Short Form -12 Evolution of mental scores over time The mental component score is determined by 4 categories of Short Form -12. The minimum value of each category is 0 and the maximun value is 100. A higher score mean better outcome Enrollment, 3 months, 6 months, 12 months
Secondary Physical component score of Short Form -12 Evolution of physical scores over time. The physical component score is determined by 4 categories of Short Form -12. The minimum value of each category is 0 and the maximun value is 100. A higher score mean better outcome Enrollment, 3 months, 6 months, 12 months
Secondary Occupational component score of Fear Avoidance Beliefs Questionnaire Evolution of occupational component score over time. Occupational component is assessed using the Fear Avoidance Beliefs Questionnaire.
The minimum value is 0 and the maximun value is 42. A higher score mean worse outcome
Enrollment, 3 months, 12 months
Secondary Physical activity component score of Fear Avoidance Beliefs Questionnaire Evolution of physical activity component score over time. Physical activity component is assessed using the Fear Avoidance Beliefs Questionnaire.
The minimum value is 0 and the maximun value is 24. A higher score mean worse outcome
Enrollment, 3 months, 12 months
Secondary Anxiety component score of Hospital Anxiety and Depression Scale Evolution of Anxiety score over time Anxiety Component is assessed using the Hospital Anxiety and Depression Scale The minimum value is 0 and the maximun value is 21. A higher score mean worse outcome Enrollment 3 months, 12 months
Secondary Depression component score of Hospital Anxiety and Depression Scale Evolution of Depression score over time Depression component is assessed using the Hospital Anxiety and Depression Scale The minimum value is 0 and the maximun value is 21. A higher score mean worse outcome Enrollment, 3 months, 12 months
Secondary Coordination care score of Patient Centered Coordination by a Care Team questionnaire Evolution of coordination care score over time This score is assessed by using Patient Centered Coordination by a Care Team questionnaire.
The minimum value is 0 and the maximun value is 42. A higher score mean better outcome
Enrollment, 3 months, 12 months
Secondary GP satisfaction related to patient care Evolution of GP satisfaction using an numerical scale The minimum value is 0 and the maximun value is 10. A higher score mean worse outcome T0 = baseline (cluster initiation); T1 = 1 year (6 months after inclusion of the 5th cluster patient); T2 = through study completion, an average of 3 years (12 months after the last cluster patient inclusion)
Secondary Physiotherapist satisfaction related to patient care Evolution of physiotherapist satisfaction using an numerical scale The minimum value is 0 and the maximun value is 10. A higher score mean worse outcome T0 = baseline (cluster initiation); T1 = 1 year (6 months after inclusion of the 5th cluster patient); T2 = through study completion, an average of 3 years (12 months after the last cluster patient inclusion)
Secondary Professionals trained for intervention number of professionals trained for intervention Baseline intervention formations
Secondary Biomechanical component score of Pain Attitudes and Beliefs score - for intervention physiotherapists Evolution of Biomechanical component score for intervention physiotherapists. Biomechanical component is assessed using the Pain Attitudes and Beliefs Score. The minimum value is 10 and the maximun value is 60. A higher score mean worse outcome T0 = baseline (cluster initiation); T1 = 1 year (6 months after inclusion of the 5th cluster patient); T2 = through study completion, an average of 3 years (12 months after the last cluster patient inclusion)
Secondary Biopsychosocial component score of Pain Attitudes and Beliefs score - for intervention physiotherapists Evolution of Biopsychosocial component score for intervention physiotherapists. Biopsychosocial component is assessed using the Pain Attitudes and Beliefs Score.The minimum value is 9 and the maximun value is 54. A higher score mean better outcome T0 = baseline (cluster initiation); T1 = 1 year (6 months after inclusion of the 5th cluster patient); T2 = through study completion, an average of 3 years (12 months after the last cluster patient inclusion)
Secondary Biopsychosocial component score of Pain Attitudes and Beliefs score - for GPs Evolution of Biopsychosocial component score for GPs. Biopsychosocial component is assessed using the Pain Attitudes and Beliefs Score.The minimum value is 9 and the maximun value is 54. A higher score mean better outcome T0 = baseline (cluster initiation); T1 = 1 year (6 months after inclusion of the 5th cluster patient); T2 = through study completion, an average of 3 years (12 months after the last cluster patient inclusion)
Secondary Biomechanical component score of Pain Attitudes and Beliefs score - for GPs Evolution of Biomechanical component score for GPs. Biomechanical component is assessed using the Pain Attitudes and Beliefs Score. The minimum value is 10 and the maximun value is 60. A higher score mean worse outcome T0 = baseline (cluster initiation); T1 = 1 year (6 months after inclusion of the 5th cluster patient); T2 = through study completion, an average of 3 years (12 months after the last cluster patient inclusion)
Secondary Professional dialogues Existence and types of dialogues between GP and other professionals during the 12 months of follow up
Secondary Number of consultations or sessions Number of consultations or sessions during the 12 months of follow up
See also
  Status Clinical Trial Phase
Completed NCT03916705 - Thoraco-Lumbar Fascia Mobility N/A
Completed NCT04007302 - Modification of the Activity of the Prefrontal Cortex by Virtual Distraction in the Lumbago N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Recruiting NCT03600207 - The Effect of Diaphragm Muscle Training on Chronic Low Back Pain N/A
Completed NCT04284982 - Periodized Resistance Training for Persistent Non-specific Low Back Pain N/A
Recruiting NCT05600543 - Evaluation of the Effect of Lumbar Belt on Spinal Mobility in Subjects With and Without Low Back Pain N/A
Withdrawn NCT05410366 - Safe Harbors in Emergency Medicine, Specific Aim 3
Completed NCT03673436 - Effect of Lumbar Spinal Fusion Predicted by Physiotherapists
Completed NCT02546466 - Effects of Functional Taping on Static Postural Control in Patients With Non-specific Chronic Low Back Pain N/A
Completed NCT00983385 - Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Chronic Low Back Pain Taking Either WHO Step I or Step II Analgesics or no Regular Analgesics Phase 3
Recruiting NCT05156242 - Corticospinal and Motor Behavior Responses After Physical Therapy Intervention in Patients With Chronic Low Back Pain. N/A
Recruiting NCT04673773 - MY RELIEF- Evidence Based Information to Support People Aged 55+ Years Living and Working With Persistent Low-back Pain. N/A
Completed NCT06049251 - ELDOA Technique Versus Lumbar SNAGS With Motor Control Exercises N/A
Completed NCT06049277 - Mulligan Technique Versus McKenzie Extension Exercise Chronic Unilateral Radicular Low Back Pain N/A
Completed NCT04980469 - A Study to Explore the Effect of Vitex Negundo and Zingiber Officinale on Non-specific Chronic Low Back Pain Due to Sedentary Lifestyle N/A
Completed NCT04055545 - High Intensity Interval Training VS Moderate Intensity Continuous Training in Chronic Low Back Pain Subjects N/A
Recruiting NCT05944354 - Wearable Spine Health System for Military Readiness
Recruiting NCT05552248 - Assessment of the Safety and Performance of a Lumbar Belt
Completed NCT05801588 - Participating in T'ai Chi to Reduce Back Pain and Improve Quality of Life N/A
Recruiting NCT05811143 - Examining the Effects of Dorsal Column Stimulation on Pain From Lumbar Spinal Stenosis Related to Epidural Lipomatosis.