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Acupuncture Treatment of Adhesive Capsulitis of the Shoulder: A Randomized Controlled Pilot Trial

  • Kim, Jung-Eun (Biomedical Research Institute, Pusan National University Hospital) ;
  • Kim, Sung-Phil (Clinical Medicine Division, Korea Institute of Oriental Medicine) ;
  • Kim, Ae-Ran (Clinical Medicine Division, Korea Institute of Oriental Medicine) ;
  • Park, Hyo-Ju (Clinical Medicine Division, Korea Institute of Oriental Medicine) ;
  • Kwon, Ojin (Clinical Medicine Division, Korea Institute of Oriental Medicine) ;
  • Jung, So-Young (Clinical Medicine Division, Korea Institute of Oriental Medicine) ;
  • Cho, Jung-Hyo (Department of Internal Korean Medicine, Dunsan Korean Medicine Hospital of Daejeon University) ;
  • Kim, Joo-Hee (Department of Acupuncture and Moxibustion Medicine, College of Korean Medicine, Sangji University) ;
  • Choi, Sun-Mi (KM Standards Center, Korea Institute of Oriental Medicine)
  • Received : 2018.07.24
  • Accepted : 2018.08.03
  • Published : 2018.08.30

Abstract

Background: Adhesive capsulitis (AC) is a common condition that includes shoulder pain and limited movement. Despite more than 100 years of AC treatment, the most efficacious treatment remains unclear. The aim of this study was to evaluate the feasibility of a randomized controlled trial (RCT) using acupuncture for AC. Methods: Thirty participants with AC were randomly assigned to acupuncture (A) or sham acupuncture (SA) groups. The participants received 15 acupuncture sessions over 6 weeks, and follow-up occurred for an additional 4 weeks thereafter. The primary clinical outcome was the numeric rating scale (NRS) for shoulder pain 6 weeks from the baseline. Secondary outcomes included range of motion (ROM) in the shoulder, the shoulder pain and disability index (SPADI), the EuroQol-5 dimensions (EQ-5D), the Pittsburgh sleep quality index (PSQI), and the patient global impression of change (PGIC). Results: Thirty participants were enrolled out of 37 screened individuals. Recruitment was conducted between August 2014 until May 2015. A total of 28 participants (93%) completed the 6-week intervention, and 26 participants (87%) completed the study. NRS, ROM, SPADI, EQ-5D, PSQI, and PGIC scores improved in both the experimental group and the sham group after 6 weeks, but the difference between the groups was not statistically significant. Adverse events were reported by 12 participants, although these events were not associated with acupuncture. Conclusion: A future RCT for AC may be feasible with some modifications to the recruitment plan and the secondary outcome measurement methods.

Keywords

References

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