Randomised controlled trial of a short course of traditional acupuncture compared with usual care for persistent non-specific low back pain

Abstract Objective To determine whether a short course of traditional acupuncture improves longer term outcomes for patients with persistent non-specific low back pain in primary care. Design Pragmatic, open, randomised controlled trial. Setting Three private acupuncture clinics and 18 general pract...

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Published in:BMJ Vol. 333; no. 7569; pp. 623 - 626
Main Authors: Thomas, K J, MacPherson, H, Thorpe, L, Brazier, J, Fitter, M, Campbell, M J, Roman, M, Walters, S J, Nicholl, J
Format: Journal Article
Language:English
Published: London British Medical Journal Publishing Group 23-09-2006
British Medical Association
BMJ Publishing Group LTD
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BMJ Publishing Group Ltd
Edition:International edition
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Summary:Abstract Objective To determine whether a short course of traditional acupuncture improves longer term outcomes for patients with persistent non-specific low back pain in primary care. Design Pragmatic, open, randomised controlled trial. Setting Three private acupuncture clinics and 18 general practices in York, England. Participants 241 adults aged 18-65 with non-specific low back pain of 4-52 weeks' duration. Interventions 10 individualised acupuncture treatments from one of six qualified acupuncturists (160 patients) or usual care only (81 patients). Main outcome measures The primary outcome was SF-36 bodily pain, measured at 12 and 24 months. Other outcomes included reported use of analgesics, scores on the Oswestry pain disability index, safety, and patient satisfaction. Results 39 general practitioners referred 289 patients of whom 241 were randomised. At 12 months average SF-36 pain scores increased by 33.2 to 64.0 in the acupuncture group and by 27.9 to 58.3 in the control group. Adjusting for baseline score and for any clustering by acupuncturist, the estimated intervention effect was 5.6 points (95% confidence interval −0.2 to 11.4) at 12 months (n = 213) and 8.0 points (2.8 to 13.2) at 24 months (n = 182). The magnitude of the difference between the groups was about 10%-15% of the final pain score in the control group. Functional disability was not improved. No serious or life threatening events were reported. Conclusions Weak evidence was found of an effect of acupuncture on persistent non-specific low back pain at 12 months, but stronger evidence of a small benefit at 24 months. Referral to a qualified traditional acupuncturist for a short course of treatment seems safe and acceptable to patients with low back pain. Trial registration ISRCTN80764175 [controlled-trials.com].
Bibliography:Correspondence to: H MacPherson
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Correspondence to: H MacPherson hm18@york.ac.uk
Ethical approval: This study was approved by York research ethics committee.
Contributors: KJT was principal investigator and grant holder. She is guarantor. KJT, HMacP, MF, JB, JPN, and MJC developed the protocol, secured initial funding, and implemented the study. HMacP, LT, and JB secured funding for the 24 months' follow-up. LT recruited patients and managed the trial. MR advised and helped recruit the general practitioners. HMacP supervised the clinical intervention. KJT, MJC, and JPN carried out the statistical analysis. SJW undertook independent statistical analysis of the primary outcomes. KJT wrote the original draft with HMacP. All authors commented on the draft and contributed to the interpretation of the findings.
We thank the patients, primary care staff, acupuncturists, and members of the trial advisory group, particularly Trevor Sheldon, Sally Bell-Sayer, and David Laverick our patient representative. © Crown copyright 2006.
Funding: This study was funded by the UK NHS Executive health technology programme. The views and opinions expressed do not necessarily reflect those of the NHS Executive. York Health Authority funded the treatment costs of the acupuncture. The National Coordinating Centre for Health Technology Assessment reviewed the protocol and the final report but had no direct involvement in the research process. KJT and JB joined the commissioning group of the National Coordinating Centre for Health Technology Assessment after funding for this study was awarded. Jon Nicholl is currently chair of the National Coordinating Centre for Health Technology Assessment commissioning group.
Competing interests: None declared.
ISSN:0959-8138
0959-8146
1468-5833
1756-1833
DOI:10.1136/bmj.38878.907361.7C