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Randomised feasibility study evaluating eye movement desensitisation and reprocessing therapy for functional neurological disorder (MODIFI)

Cope, SR; Smith, JG; El-Leithy, S; Vanzan, S; Hogwood, P; Golder, D; Turner, KJ; Crowley, M; Billings, J; Pick, S; et al. Cope, SR; Smith, JG; El-Leithy, S; Vanzan, S; Hogwood, P; Golder, D; Turner, KJ; Crowley, M; Billings, J; Pick, S; Pentland, C; Edwards, MJ (2025) Randomised feasibility study evaluating eye movement desensitisation and reprocessing therapy for functional neurological disorder (MODIFI). Journal of Neurology, 272 (8). p. 493. ISSN 0340-5354 https://doi.org/10.1007/s00415-025-13219-5
SGUL Authors: Smith, Jared Grant

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Abstract

Background Functional neurological disorder (FND) is a common neurological presentation with symptoms such as seizures, walking difficulties, limb weakness and cognitive difficulties. Treatments for FND include physiotherapy and psychological therapy. Eye movement desensitisation and reprocessing therapy (EMDR) is a therapy designed to reduce disturbance associated with distressing or traumatic memories. Case report evidence suggests possible benefit for people with FND. This randomised feasibility study aimed to assess whether a large-scale trial evaluating EMDR for FND would be feasible and acceptable. Methods Fifty participants with FND were randomised to either FND-focused EMDR plus standard neuropsychiatric care (NPC) or NPC alone. Feasibility criteria were recruitment rate, intervention adherence, and outcome measure completion. Assessment of safety was also examined, as well as therapy satisfaction. Participants completed questionnaires at baseline, 3 months, 6 months and 9 months. FND symptoms were assessed using Ecological Momentary Assessment at each time point. Results Recruitment rate was 58%, intervention adherence was 88%, and outcome measure completion was 68% for Ecological Momentary Assessment and 76% for questionnaires at 9-month follow-up. Participants experienced functional motor symptoms (80%), functional seizures (64%), and cognitive symptoms (32%). Participants receiving EMDR + NPC reported greater satisfaction and greater FND improvement compared to NPC. Questionnaire data suggested greater reductions in PTSD, depression, anxiety, dissociation, disability and healthcare-use for EMDR + NPC. Discussion The study demonstrated that an FND-specific protocol for EMDR was feasible and acceptable. Potential positive effects on FND symptoms, mental health, disability, and healthcare utilisation were found. A full-scale trial is warranted to establish efficacy. Trial Registration NCT05455450 (www.clinicaltrials.gov).

Item Type: Article
Additional Information: © The Author(s) 2025 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Keywords: Humans, Nervous System Diseases, Treatment Outcome, Follow-Up Studies, Feasibility Studies, Adult, Aged, Middle Aged, Female, Male, Young Adult, Eye Movement Desensitization Reprocessing, Outcome Assessment, Health Care
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Journal of Neurology
ISSN: 0340-5354
Language: en
Media of Output: Electronic
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
202277National Institute for Health and Care Researchhttps://doi.org/10.13039/501100000272
PubMed ID: 40627223
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/117704
Publisher's version: https://doi.org/10.1007/s00415-025-13219-5

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