"Evaluation of the Effectiveness of the MDT Method (Mechanical Diagnosis and Therapy) in the Management of Low Back Pain in the Subacute Phase"
NCT ID: NCT03720444
Last Updated: 2018-10-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
10 participants
OBSERVATIONAL
2019-01-01
2019-05-01
Brief Summary
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Few studies have specifically evaluated the effectiveness of the MDT method in the subacute phase, a phase that appears to be crucial before the chronicization of low back pain.
The main objective of this study will be to evaluate the pain of patients managed by the MDT method.
The analysis of the main criterion (Visual Analog Scale) will be done using a type individual clinical trial specific: the Single Case Experimental Design or SCED in lines of multiple bases.
This type of study makes it possible to carry out a comparative test on a single subject acting as its own witness in order to obtain an acceptable level of evidence response for that particular patient.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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MDT (mechanical diagnosis and therapy) method
MDT (mechanical diagnosis and therapy) method
The intervention consists of a first session to carry out an assessment, followed by 4 reassessment sessions
Interventions
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MDT (mechanical diagnosis and therapy) method
The intervention consists of a first session to carry out an assessment, followed by 4 reassessment sessions
Eligibility Criteria
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Inclusion Criteria
* Aged 18 to 55 years old
* Suffering from common-looking low back pain. Low back pain is defined as pain or localized discomfort under the 12th dorsal vertebrae and above the inner fold buttock, with possible irradiation to the lower limb but not exceeding the knee.
* Evolving for 4 to 12 weeks (subacute period).
* Period preceded by a period of 30 days without low back pain (in order to avoid recurrent low back pain, rather similar to the chronic phase).
Exclusion Criteria
* Irradiation below the knee
* Patient knowing she is pregnant
* Protected adults
* Patient with proven cognitive impairment
* Patient with a decompensated psychiatric pathology
* Incapacity to consent
* Refusal to participate in the study
18 Years
55 Years
ALL
No
Sponsors
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Nantes University Hospital
OTHER
Responsible Party
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Principal Investigators
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Celine BOUTON, Professor
Role: PRINCIPAL_INVESTIGATOR
Nantes University
Locations
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Picasso physiotherapy cabinet (5 rue Nina Simone - 44 000 NANTES)
Nantes, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RC18_ 0269
Identifier Type: -
Identifier Source: org_study_id
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