Treatment of Chronic Low Back Pain: A Trial Comparing Traditional Back School and Individual Therapist-Assisted Exercise

NCT00256373 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL

Last updated 2006-04-19

No results posted yet for this study

Summary

Rheumatologists are discussing, whether rehabilitation of patients with low back pain (LBP) can be improved. At present patients with LBP start treatment as soon as possible, this also applies for patients with chronic low back pain (CLBP) - pain lasting over 12 weeks. At Glostrup University Hospital department of Physical Medicine/rheumatology we use a method (method A) where an interdisciplinary team gives the patients a treatment composed of various topics. This includes among other things education, physical team training, exercises in swimming pool, stretching exercises, and occupational therapy. A different method (method B) originates from the Rehabilitation centre in Karlslunde led by Teddy Oefeldt. Here they focus strictly on dynamic training of muscles in the back and the buttocks. A therapist, who in the beginning partly carries the patient through the exercises, assists this training.

In both methods, individually considerations are taken, but to a greater extend in method B. The treatment will extend over a three months period.

A few earlier investigations have compared these two methods, but they have not been systematized to such a degree, that they gave any final conclusions. Therefore, we initialized an investigation including a larger number of patients, where the two methods are compared from the results the patients achieve after 3, 6, 12 and 24 months.

286 consecutive patients were included and randomized to one of the two methods. Those, who did not wish to participate in the investigation, were treated according to the department's normal procedure (Method A)

Conditions

  • Chronic Low Back Pain

Interventions

PROCEDURE

Mod. functional restoration-Individ. dynamic back-muscle

Sponsors & Collaborators

  • Sygekassernes Helsefond

    collaborator OTHER
  • Apotekerfonden af 1991

    collaborator OTHER
  • Indenrigs- og sundhedsministeriet

    collaborator UNKNOWN
  • University Hospital, Gentofte, Copenhagen

    lead OTHER

Principal Investigators

  • Charlotte Lundsgaard, MD

  • Claus Hellesen, MD

  • Alex Oefeldt, Therapist

  • Gorm Thamsborg, Dr.Med.Sci.

  • Arne Astrup, Dr.Med.Sci.

  • Steen Stender, Dr.Med.Sci.

  • Ninna Dufour, MD · Unfilliated

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-01-31
Completion
2005-11-30

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00256373 on ClinicalTrials.gov