A Randomized, Single-Blind, Placebo-Controlled Study on the Efficacy of the Arthrokinematic Approach-Hakata Method in Patients with Chronic Nonspecific Low Back Pain
- PMID: 26646534
- PMCID: PMC4672908
- DOI: 10.1371/journal.pone.0144325
A Randomized, Single-Blind, Placebo-Controlled Study on the Efficacy of the Arthrokinematic Approach-Hakata Method in Patients with Chronic Nonspecific Low Back Pain
Abstract
Study design: Cized, single-blind, controlled trial.
Objective: To investigate the efficacy of the Arthrokinematic approach (AKA)-Hakata (H) method for chronic low back pain.
Summary of background data: The AKA-H method is used to manually treat abnormalities of intra-articular movement.
Methods: One hundred eighty-six patients with chronic nonspecific low back pain randomly received either the AKA-H method (AKA-H group) or the sham technique (S group) monthly for 6 months. Data were collected at baseline and once a month. Outcome measures were pain intensity (visual analogue scale [VAS]) and quality of life (the Roland-Morris Disability Questionnaire [RDQ] and Short Form SF-36 questionnaire [SF-36]).
Results: At baseline, the VAS, RDQ, and SF-36 scores showed similar levels between the groups. After 6 months, the AKA-H group had more improvement in the VAS (42.8% improvement) and RDQ score (31.1% improvement) than the sham group (VAS: 10.4% improvement; RDQ: 9.8% improvement; both, P < 0.001). The respective scores for the SF-36 subscales (physical functioning, role physical, bodily pain, social functioning, general health perception, role emotional, and mental health) were also significantly more improved in the AKA-H group than in the sham group (all, P < 0.001). The scores for the physical, psychological, and social aspects of the SF-36 subscales showed similar improvement in the AKA-H group.
Conclusion: The AKA-H method can be effective in managing chronic low back pain.
Trial registration: UMIN Clinical Trials Registry (UMIN-CTR) UMIN000006250.
Conflict of interest statement
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