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Acupuncture atHouxi(SI 3) acupoint for acute neck pain caused by stiff neck: study protocol for a pilot randomised controlled trial

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IntroductionThe use of acupuncture has been suggested for the treatment of acute neck pain caused by stiff neck in China. However, current evidence is insufficient to draw any conclusions about its efficacy. Therefore this pilot study was designed to evaluate the feasibility and efficacy of acupuncture at theHouxi(SI3) acupoint for treatment of acute neck pain.Methods/analysisThis pilot study will be a two-parallel-group, assessor-blinded, randomised controlled trial. Thirty-six stiff neck participants with acute neck pain will be recruited and randomly divided into two groups in a 1:1 ratio. Participants in the control group will receive massage on the local neck region (5 min each session, three times a day for 3 days). In addition to massage, patients in the treatment group will receive acupuncture (one session a day for 3 days). Measures will be taken at 0, 3 and 15 days. The primary outcome is the Northwick Park Neck Pain Questionnaire (NPQ). The secondary outcome is the Short Form of the McGill Pain Questionnaire (SF-MPQ).Ethics/disseminationThe protocol for this pilot randomised clinical trial has undergone ethics scrutiny and been approved by the ethics review boards of the First Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine (Permission number: HZYLL201303502). The findings of this study will provide important clinical evidence on the feasibility and efficacy of acupuncture treatment for stiff neck patients with acute neck pain. In addition, it will explore the feasibility of further acupuncture research.Trial registration numberChiCTR-TRC-13003911.
Title: Acupuncture atHouxi(SI 3) acupoint for acute neck pain caused by stiff neck: study protocol for a pilot randomised controlled trial
Description:
IntroductionThe use of acupuncture has been suggested for the treatment of acute neck pain caused by stiff neck in China.
However, current evidence is insufficient to draw any conclusions about its efficacy.
Therefore this pilot study was designed to evaluate the feasibility and efficacy of acupuncture at theHouxi(SI3) acupoint for treatment of acute neck pain.
Methods/analysisThis pilot study will be a two-parallel-group, assessor-blinded, randomised controlled trial.
Thirty-six stiff neck participants with acute neck pain will be recruited and randomly divided into two groups in a 1:1 ratio.
Participants in the control group will receive massage on the local neck region (5 min each session, three times a day for 3 days).
In addition to massage, patients in the treatment group will receive acupuncture (one session a day for 3 days).
Measures will be taken at 0, 3 and 15 days.
The primary outcome is the Northwick Park Neck Pain Questionnaire (NPQ).
The secondary outcome is the Short Form of the McGill Pain Questionnaire (SF-MPQ).
Ethics/disseminationThe protocol for this pilot randomised clinical trial has undergone ethics scrutiny and been approved by the ethics review boards of the First Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine (Permission number: HZYLL201303502).
The findings of this study will provide important clinical evidence on the feasibility and efficacy of acupuncture treatment for stiff neck patients with acute neck pain.
In addition, it will explore the feasibility of further acupuncture research.
Trial registration numberChiCTR-TRC-13003911.

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