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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00939107
Other study ID # KF-01-057/03
Secondary ID
Status Completed
Phase N/A
First received July 13, 2009
Last updated November 9, 2009
Start date September 2003
Est. completion date November 2008

Study information

Verified date November 2009
Source Back and Rehabilitation Center, Copenhagen
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Introduction:

The McKenzie method as well as spinal manipulation is commonly used for the treatment of low back pain throughout the western world. Recently, the need for studies testing the effect of treatment strategies to specific diagnostic subgroups of patients has been emphasized. The present study aims to compare the effectiveness of the McKenzie method and chiropractic manipulation, information, and advice for patients with clinical signs of persistent symptoms originating from a diskus in the low back.

Methods:

After clinical screening 350 patients with or without leg pain who presented with centralization of symptoms or signs of disc herniation were randomized to the McKenzie group or the manipulation group. The outcome measures, Roland Morris Disability Questionnaire, 11 point numerical pain scale, 6 point global perceived change scale, and quality of life (Short Form-36) were assessed at baseline, at end of treatment, and at 2 and 12 months follow-up.


Description:

In 1998, Cherkin et al. published a study showing no difference between outcomes following the McKenzie method, chiropractic manipulation, or the provision of an educational booklet for the treatment of patients with acute non-specific low back pain. Recently, the need for studies testing the effect of treatment strategies to specific diagnostic subgroups of patients has been emphasized. The present study aims to compare the effectiveness of the McKenzie method and chiropractic manipulation, information, and advice for patients with clinical signs of disc-related symptoms for duration of more than 6 Weeks.


Recruitment information / eligibility

Status Completed
Enrollment 350
Est. completion date November 2008
Est. primary completion date November 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- 18 to 60 years of age

- suffering from low back pain (LBP) with or without leg pain for a period of more than 6 weeks

- able to speak and understand the Danish language

- with a presentation of clinical signs of disc-related symptoms.

Exclusion Criteria:

- positive non-organic signs

- serious pathology suspected based on physical examination and/or magnetic resonance imaging

- application for disability pension or pending litigation

- pregnancy

- comorbidity

- recent back surgery

- problems with communication

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
spinal manipulation
Spinal manipulation to the lumbopelvic spine in combination with information about examination findings and advice about back care
McKenzie exercises
McKenzie exercises according to the principles of Mechanical Diagnosis and Therapy

Locations

Country Name City State
Denmark Back and Rehabilitation Center Copengagen Copenhagen Copenhagen OE

Sponsors (5)

Lead Sponsor Collaborator
Back and Rehabilitation Center, Copenhagen Foundation for Chiropractic Research and Post Graduate Education, The Danish Institute for Mechanical Diagnosis and Therapy., The Danish Physiotherapy Organization., The Danish Rheumatism Association

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disability two months after treatment No
Primary Number of Patients With Treatment Success Two months posttreatment No
Secondary Pain twelve months posttreatment No
Secondary Number of Patients on Sick Leave twelve months posttreatment No
Secondary Quality of Life twelve months posttreatment No
Secondary Cost Effectiveness twelve months posttreatment No
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