Functional MRI Neurofeedback Outperforms Cognitive Behavioral Therapy for Reducing Tinnitus Distress: A Prospective Randomized Clinical Trial.

Radiology

From the Medical Image Processing Laboratory, Neuro-X Institute, École Polytechnique Fédérale de Lausanne, Campus Biotech, Chemin des Mines 9, Geneva 1202, Switzerland (N.G., D.V.D.V.); Department of Radiology and Medical Informatics (N.G., D.V.D.V.) and Department of Medicine (S.H.), University of Geneva, Geneva, Switzerland; Department of Neurology, Psychosomatic Medicine Unit, Inselspital Bern University Hospital, University of Bern, Bern, Switzerland (N.G.); Wyss Center for Bio and Neuroengineering, Campus Biotech, Geneva, Switzerland (S.T., A.Y.); Service of Otorhinolaryngology-Head and Neck Surgery, Department of Clinical Neurosciences (D.D., L.G., J.V., F.V., P.S.) and Department of Psychiatry (C.L.R., A.S.), Geneva University Hospitals, Geneva, Switzerland; Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, Tenn (R.S.); Centre d'Imagerie Médicale de Cornavin, Geneva, Switzerland (S.H.); and Department of Surgical Sciences, Radiology, Uppsala University, Uppsala, Sweden (S.H.).

Published: February 2024

Background Cognitive behavioral therapy (CBT) is the current standard treatment for chronic severe tinnitus; however, preliminary evidence suggests that real-time functional MRI (fMRI) neurofeedback therapy may be more effective. Purpose To compare the efficacy of real-time fMRI neurofeedback against CBT for reducing chronic tinnitus distress. Materials and Methods In this prospective controlled trial, participants with chronic severe tinnitus were randomized from December 2017 to December 2021 to receive either CBT (CBT group) for 10 weekly group sessions or real-time fMRI neurofeedback (fMRI group) individually during 15 weekly sessions. Change in the Tinnitus Handicap Inventory (THI) score (range, 0-100) from baseline to 6 or 12 months was assessed. Secondary outcomes included four quality-of-life questionnaires (Beck Depression Inventory, Pittsburgh Sleep Quality Index, State-Trait Anxiety Inventory, and World Health Organization Disability Assessment Schedule). Questionnaire scores between treatment groups and between time points were assessed using repeated measures analysis of variance and the nonparametric Wilcoxon signed rank test. Results The fMRI group included 21 participants (mean age, 49 years ± 11.4 [SD]; 16 male participants) and the CBT group included 22 participants (mean age, 53.6 years ± 8.8; 16 male participants). The fMRI group showed a greater reduction in THI scores compared with the CBT group at both 6 months (mean score change, -28.21 points ± 18.66 vs -12.09 points ± 18.86; = .005) and 12 months (mean score change, -30 points ± 25.44 vs -4 points ± 17.2; = .01). Compared with baseline, the fMRI group showed improved sleep (mean score, 8.62 points ± 4.59 vs 7.25 points ± 3.61; = .006) and trait anxiety (mean score, 44 points ± 11.5 vs 39.84 points ± 10.5; = .02) at 1 month and improved depression (mean score, 13.71 points ± 9.27 vs 6.53 points ± 5.17; = .01) and general functioning (mean score, 24.91 points ± 17.05 vs 13.06 points ± 10.1; = .01) at 6 months. No difference in these metrics over time was observed for the CBT group ( value range, .14 to >.99). Conclusion Real-time fMRI neurofeedback therapy led to a greater reduction in tinnitus distress than the current standard treatment of CBT. ClinicalTrials.gov registration no.: NCT05737888; Swiss Ethics registration no.: BASEC2017-00813 © RSNA, 2024

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http://dx.doi.org/10.1148/radiol.231143DOI Listing

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