A randomised controlled feasibility trial of intermittent theta burst stimulation with an open longer‐term follow‐up for young people with persistent anorexia nervosa (RaISE): Study protocol

Author:

Hemmings Amelia1ORCID,Gallop Lucy1,İnce Başak1,Cutinha Darren2,Kan Carol3,Simic Mima2,Zadeh Ewa4,Malvisi Isabella5,McKenzie Katie5,Zocek Lucy5,Sharpe Helen6,O’Daly Owen7,Campbell Iain C.1,Schmidt Ulrike12

Affiliation:

1. Centre for Research in Eating and Weight Disorders (CREW) Department of Psychological Medicine King's College London Institute of Psychiatry, Psychology and Neuroscience London UK

2. South London and Maudsley NHS Foundation Trust London UK

3. Central and North West London NHS Foundation Trust London UK

4. South West London and St Georges Mental Health NHS Trust London UK

5. EDIFY London UK

6. School of Health in Social Science University of Edinburgh Edinburgh UK

7. Department of Neuroimaging Centre for Neuroimaging Sciences King's College London Institute of Psychiatry Psychology and Neuroscience London UK

Abstract

AbstractObjectiveWe present the protocol of a feasibility randomised controlled trial (RCT) of intermittent theta burst stimulation (iTBS) for young people with anorexia nervosa (AN). Effective first‐line psychological therapies exist for young people with AN, but little is known about how to treat those who do not respond. Non‐invasive neuromodulation, such as iTBS, could address unmet treatment needs by targeting neurocircuitry associated with the development and/or maintenance of AN.DesignSixty‐six young people (aged 13–30 years) with persistent AN will be randomly allocated to receive 20 sessions of real or sham iTBS over the left dorsolateral prefrontal cortex in addition to their usual treatment. Outcomes will be measured at baseline, post‐treatment (1‐month post‐randomisation) and 4‐months post‐randomisation (when unblinding will occur). Additional open follow‐ups will be conducted at 12‐ and 24‐months post‐randomisation. The primary feasibility outcome is the proportion of participants retained in the study at 4‐months. Secondary outcomes include AN symptomatology, other psychopathology, quality of life, service utilisation, neurocognitive processes, and neuroimaging measures.DiscussionFindings will inform the development of a future large‐scale RCT. They will also provide exploratory data on treatment efficacy, and neural and neurocognitive predictors and correlates of treatment response to iTBS in AN.

Funder

Economic and Social Research Council

Medical Research Council

Arts and Humanities Research Council

UK Research and Innovation

Publisher

Wiley

Subject

Psychiatry and Mental health,Clinical Psychology

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