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Effects of Eye Movement Desensitization and Reprocessing (EMDR) Treatment in Chronic Pain Patients: A Systematic Review

Objective This study systematically reviewed the evidence regarding the effects of eye movement desensitization and reprocessing (EMDR) therapy for treating chronic pain. Design Systematic review. Methods We screened MEDLINE, EMBASE, the Cochrane Library, CINHAL Plus, Web of Science, PsycINFO, PSYND...

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Published in:Pain medicine (Malden, Mass.) Mass.), 2014-02, Vol.15 (2), p.247-263
Main Authors: Tesarz, Jonas, Leisner, Sabine, Gerhardt, Andreas, Janke, Susanne, Seidler, Günter H., Eich, Wolfgang, Hartmann, Mechthild
Format: Article
Language:English
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Summary:Objective This study systematically reviewed the evidence regarding the effects of eye movement desensitization and reprocessing (EMDR) therapy for treating chronic pain. Design Systematic review. Methods We screened MEDLINE, EMBASE, the Cochrane Library, CINHAL Plus, Web of Science, PsycINFO, PSYNDEX, the Francine Shapiro Library, and citations of original studies and reviews. All studies using EMDR for treating chronic pain were eligible for inclusion in the present study. The main outcomes were pain intensity, disability, and negative mood (depression and anxiety). The effects were described as standardized mean differences. Results Two controlled trials with a total of 80 subjects and 10 observational studies with 116 subjects met the inclusion criteria. All of these studies assessed pain intensity. In addition, five studies measured disability, eight studies depression, and five studies anxiety. Controlled trials demonstrated significant improvements in pain intensity with high effect sizes (Hedges' g: −6.87 [95% confidence interval (CI95): −8.51, −5.23] and −1.12 [CI95: −1.82, −0.42]). The pretreatment/posttreatment effect size calculations of the observational studies revealed that the effect sizes varied considerably, ranging from Hedges' g values of −0.24 (CI95: −0.88, 0.40) to −5.86 (CI95: −10.12, −1.60) for reductions in pain intensity, −0.34 (CI95: −1.27, 0.59) to −3.69 (CI95: −24.66, 17.28) for improvements in disability, −0.57 (CI95: −1.47, 0.32) to −1.47 (CI95: −3.18, 0.25) for improvements in depressive symptoms, and −0.59 (CI95: −1.05, 0.13) to −1.10 (CI95: −2.68, 0.48) for anxiety. Follow‐up assessments showed maintained improvements. No adverse events were reported. Conclusions Although the results of our study suggest that EMDR may be a safe and promising treatment option in chronic pain conditions, the small number of high‐quality studies leads to insufficient evidence for definite treatment recommendations.
ISSN:1526-2375
1526-4637
DOI:10.1111/pme.12303