Day-to-Day Changes of Auricular Point Acupressure to Manage Chronic Low Back Pain: A 29-day Randomized Controlled Study

被引:37
作者
Yeh, Chao Hsing [1 ]
Suen, Lorna Kwai-Ping [2 ]
Chien, Lung-Chang [3 ]
Margolis, Leah [1 ]
Liang, Zhan [1 ]
Glick, Ronald M. [4 ,5 ,6 ]
Morone, Natalia E. [7 ]
机构
[1] Univ Pittsburgh, Sch Nursing, Pittsburgh, PA 15261 USA
[2] Hong Kong Polytech Univ, Sch Nursing, Hong Kong, Hong Kong, Peoples R China
[3] Univ Texas Hlth Sci Ctr San Antonio, Sch Publ Hlth San Antonio, Dept Biostat, Res Adv Community Hlth Ctr, San Antonio, TX USA
[4] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15261 USA
[5] Univ Pittsburgh, Sch Med, Dept Phys Med, Pittsburgh, PA 15261 USA
[6] Univ Pittsburgh, Sch Med, Dept Rehabil, Pittsburgh, PA 15261 USA
[7] Univ Pittsburgh, Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Dept Med,Div Gen Internal Med,Vet Adm,Sch Med, Pittsburgh, PA 15261 USA
关键词
Auricular Point Acupressure; Chronic Low Back Pain; Pain Intensity; Analgesic Use; EVIDENCE-INFORMED MANAGEMENT; ACUPUNCTURE; PROTOCOL; PREVALENCE; RELIEF; RECALL;
D O I
10.1111/pme.12789
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
ObjectiveThe purpose of this study was to determine the effects of a 4-week auricular point acupressure (APA) treatment on chronic low back pain (CLBP) outcomes and examine the day-to-day variability of CLBP in individuals receiving APA for CLBP over 29 days. DesignThis was a prospective, randomized controlled trial (RCT). Data were collected at baseline, during each of the four office visits for APA treatment, after the completion of the 4-week intervention, and 1 month after the last treatment. A daily diary was given to each participant to record his or her APA practices, analgesic use, and pain intensity. InterventionsAPA was used to manage CLBP. The participants received one APA treatment per week for 4 weeks. Patients and Setting. Sixty-one participants with CLBP were randomized into either a real APA or sham APA treatment group. Participants were recruited from primary care offices and clinics or through the Research Participant Registry at the University of Pittsburgh. ResultsAmong participants in the real APA group, a 30% reduction of worst pain was exhibited after the first day of APA treatment, and continuous reduction in pain (44%) was reported by the completion of the 4-week APA. This magnitude of pain reduction reached the clinically significant level of improvement reported in other clinical trials of chronic pain therapies. Analgesic use by participants in the real APA group also was reduced compared with use by participants in the sham group. ConclusionThis study shows that APA is a promising pain management strategy that is not invasive and can be self-managed by participants for CLBP. Given the day-to-day fluctuation in ratings, the tighter ecologic assessment of pain scores and other treatment parameters are an important pragmatic aspect of the design of chronic pain studies.
引用
收藏
页码:1857 / 1869
页数:13
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