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The effect of dry needling on the radiating pain in subjects with discogenic low-back pain: a randomized control trial
Mahmoudzadeh A, Rezaeian ZS, Karimi A, Dommerholt J
Journal of Research in Medical Sciences 2016;21(86):Epub
clinical trial
7/10 [Eligibility criteria: Yes; Random allocation: Yes; Concealed allocation: No; Baseline comparability: Yes; Blind subjects: No; Blind therapists: No; Blind assessors: Yes; Adequate follow-up: Yes; Intention-to-treat analysis: Yes; Between-group comparisons: Yes; Point estimates and variability: Yes. Note: Eligibility criteria item does not contribute to total score] *This score has been confirmed*

BACKGROUND: Disk herniation is the most common cause of radiating low back pain (LBP) in subjects under 60 years of age. The present study aims to compare the effect of dry needling (DN) and a standard conservative approach on the pain and function in subjects with discogenic radiating LBP. MATERIALS AND METHODS: Fifty-eight subjects with discogenic radicular LBP were screened and randomized into control (standard physical therapy, n = 29) and experimental group (standard physical therapy and DN, n = 29). Radiating pain intensity and disability were measured using visual analog scale (VAS) and Oswestry Disability indices at baseline, at the end of treatment and 2 months after the last intervention session. The changes in pain intensity and disability were studied using a 3x2 repeated measures analysis of variance considering time as the within-subject factor and group as the between-subject. RESULTS: Pain intensity and disability scores decreased significantly in both experimental and control groups (experimental group VAS = 37.24, Oswestry Disability Index (ODI) 28.48, control group VAS 45.5, ODI 32.96), following the intervention. The change continued during the follow-up period (p < 0.001 for all comparisons). Pain and disability improvement, however, were more significant in experimental group, both in post intervention (experimental group VAS 25.17, ODI 22.17, control group VAS 42.4, ODI 30.27) (p = 0.05 and p = 0.03, respectively) and follow-up measures (p = 0.006 and p = 0.002, respectively). CONCLUSION: Both intervention strategies seem to significantly improve pain and disability immediately following intervention, where the improvement continued during 2 months after the last active intervention. Therefore, supplementary DN application may enhance the effect of the standard intervention considerably.

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