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International Journal of Clinical Pharmacology & Pharmacotherapy Volume 1 (2016), Article ID 1:IJCPP-115, 5 pages
https://doi.org/10.15344/2456-3501/2016/115
Research Article
Osteopathic Treatment of Patients Suffering from Chronic Non-specific Low Back Pain: A Dose- response Pilot Study

Espen Glomsrød1*, Stig Larsen2 and Roar Jensen2,3

1Department of of Global Health and Primary Care, University of Bergen Norway
2Professor in controlled clinical research methodology and statistics, Faculty of veterinary medicine, University of Life Sciences Oslo, Norway
3Physiotherapy research Group, Department of Global Health and Primary Care, University of Bergen Norway
Dr. Espen Glomsrød, Department of of Global Health and Primary Care, University of Bergen, Stigveien 16, 1785 Halden, Norway; E-mail: eglom@halden.net
29 May 2016; 27 July 2016; 29 July 2016
Glomsrød E, Larsen S, Jensen R (2016) Osteopathic Treatment of Patients Suffering from Chronic Non-specific Low Back Pain: A Dose- response Pilot Study. Int J Clin Pharmacol Pharmacother 1: 115. doi: https://doi.org/10.15344/2456-3501/2016/115

Abstract

Background: Dose- response studies are needed for pharmaceuticals, but have not been commonly performed in the field of manual therapy.
Objective: The aim of this study was to determine the combination of treatment numbers and intervals needed to obtain the optimal effect of osteopathic treatment for patients with chronic non-specific low back pain and to highlight methodological aspects concerning dose-response studies in the field of manual therapies.
Design: The study was performed as an open, randomized, single -centre trial with a 22 factorial design.
Methods: The patients were allocated equally to four groups by block randomization. The first group was given two treatments at an interval of 14 days, the second group was given two treatments at an interval of seven days, the third group received four treatments with intervals of 14 days, and the fourth group received four treatments with intervals of seven days. Oswestry Disability Index (ODI) and the Numeric Pain Rating Scale (NPRS) were recorded at baseline and two weeks post treatment.
Participants: Eight women and four men with chronic non-specific low back pain were included.
Results: The two treatments with an interval of 14 days resulted in an ODI reduction of only 1.3 (95% CI: -21 – 24.1). The largest reduction in ODI was detected in the four treatments with the seven days intervals. The mean reduction in this group was found to be 19.3 (95% CI: -14.4 – 53.1). An interaction between the number of treatments and the treatment interval was observed.
Conclusion: The effect increased with increases in the numbers of treatment and reductions in the treatment interval. The program with four treatments and intervals of seven days was found to be optimal among the four examined regimens.