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한의약융합데이터센터


근거중심한의약 DB

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Title

Spinal Manipulative Therapy-Specific Changes in Pain Sensitivity in Individuals With Low Back Pain (NCT01168999).

Authors

Bialosky JE, George SZ, Horn ME, Price DD, Staud R, Robinson ME.

Journal

J Pain.

Year

2014

Vol (Issue)

15(2)

Page

136-48.

doi

10.1016/j.jpain.2013.10.005.

PMID

24361109

Url

http://www.ncbi.nlm.nih.gov/pubmed/24361109

MeSH

Adult
Central Nervous System Sensitization
Disability Evaluation
Female
Hot Temperature
Humans
Low Back Pain/psychology
Low Back Pain/therapy*
Male
Musculoskeletal Manipulations*/psychology
Pain Measurement
Pain Threshold
Patient Satisfaction
Surveys and Questionnaires
Time Factors
Treatment Outcome

Keywords

Central sensitization; low back pain; manual therapy; placebo; spinal manipulation

한글 키워드

중추 감작; 요통; 도수 치료; 플라시보; 척추 도수치료

KMCRIC
Summary & Commentary

KMCRIC 비평 보기 +

Korean Study

Abstract

Spinal manipulative therapy (SMT) is effective for some individuals experiencing low back pain; however, the mechanisms are not established regarding the role of placebo. SMT is associated with changes in pain sensitivity, suggesting related altered central nervous system response or processing of afferent nociceptive input. Placebo is also associated with changes in pain sensitivity, and the efficacy of SMT for changes in pain sensitivity beyond placebo has not been adequately considered. We randomly assigned 110 participants with low back pain to receive SMT, placebo SMT, placebo SMT with the instructional set ""The manual therapy technique you will receive has been shown to significantly reduce low back pain in some people,"" or no intervention. Participants receiving the SMT and placebo SMT received their assigned intervention 6 times over 2 weeks. Pain sensitivity was assessed prior to and immediately following the assigned intervention during the first session. Clinical outcomes were assessed at baseline and following 2 weeks of participation in the study. Immediate attenuation of suprathreshold heat response was greatest following SMT (P = .05, partial η(2) = .07). Group-dependent differences were not observed for changes in pain intensity and disability at 2 weeks. Participant satisfaction was greatest following the enhanced placebo SMT. This study was registered at www.clinicaltrials.gov under the identifier NCT01168999.
PERSPECTIVE:
The results of this study indicate attenuation of pain sensitivity is greater in response to SMT than the expectation of receiving an SMT. These findings suggest a potential mechanism of SMT related to lessening of central sensitization and may indicate a preclinical effect beyond the expectations of receiving SMT.

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