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Clinical Trials/NCT00454792
NCT00454792
Completed
Not Applicable

Rehabilitation of Patients With Modic Changes in the Lumbar Spine - a Randomized Controlled Trial

The Back Research Center, Denmark1 site in 1 country100 target enrollmentMarch 2007
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
The Back Research Center, Denmark
Enrollment
100
Locations
1
Primary Endpoint
The primary outcome measure is actual LBP, as measured with an "11 point box scale".
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to compare patients with low back pain (LBP) and Modic Changes from The Backcenter Funen, Ringe:

  1. To compare the effect of two types of non-operative treatments:

    A. exercise and advice to be physically active

    B. restitution and advice not to overload the spine

  2. To investigate if the results of the treatment are influenced by gender, age, smoking, and physical load.

Detailed Description

The clinical experience is that many patients with Modic changes have relatively severe and persistent LBP, which typically appears to be resistant to treatment. Furthermore, a retrospective study at The Backcenter Funen, Ringe, shows that patients with MC fail to improve engaging physical activity. This is unfortunate, because the typical rehabilitation for patients with persistent LBP is back exercises and information about keeping physically active. This means that this relatively large subgroup of patients with Modic changes probably does not improve with the rehabilitation tools used today. A randomised controlled trial has therefore been designed to study the specific subgroup of patients with Modic changes. In this study we will compare the present "state-of-the art" rehabilitation approach to persistent LBP (namely to exercise and keep active) with a new concept (restitution). The justification for this is that restitution reduces mechanical stress on the vertebrae and therefore would allow heeling of the possible micro fractures in Modic changes.

Registry
clinicaltrials.gov
Start Date
March 2007
End Date
September 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
The Back Research Center, Denmark
Responsible Party
Principal Investigator
Principal Investigator

Rikke Krüger Jensen

MSc

The Back Research Center, Denmark

Eligibility Criteria

Inclusion Criteria

  • Primary inclusion criteria for receiving MRI
  • The patient must have LBP with a current duration of 3 - 12 month.
  • The patient must have an actual pain intensity ≥4 on numerical pain rating scale from 0-
  • Secondary inclusion criteria for receiving MRI
  • The patient must speak and understand Danish.
  • The patient must be between 18-60 years of age.
  • The patient must be willing to participate in the project. Inclusions criterium for the project
  • There must be an MRI showing MC in the lumbar spine.

Exclusion Criteria

  • The patient is unable to go through with the project because of other physical or mental disorder.
  • The patient is pregnant.
  • The patient is referred to operation.

Outcomes

Primary Outcomes

The primary outcome measure is actual LBP, as measured with an "11 point box scale".

Time Frame: 10 weeks and 12 months

Secondary Outcomes

  • General Health, as measured with the EQ-5D (EuroQol)(10 weeks and 12 months)
  • General improvement, as measured with two global instruments a 7-point transition question and an assessment score consisting of a "bothersomeness index"(10 weeks and 12 months)
  • Physical functions measured with "Roland Morris Disability Questionnaire"(10 weeks and 12 months)

Study Sites (1)

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