Low-intensity repetitive transcranial magnetic stimulation is safe and well tolerated by people living with MS – outcomes of the phase I randomised controlled trial (TAURUS)

Author:

Nguyen Phuong Tram1ORCID,Zarghami Amin1ORCID,Makowiecki Kalina1ORCID,Stevens Natasha1ORCID,Ezegbe Chigozie1,Kyle Kain2,Wang Chenyu2,Ly Linda2,De La Rue Katie1,Hinder Mark R3,Johnson Lewis1,Rodger Jennifer4,Cooper Samantha5,Cullen Carlie L1ORCID,Barnett Michael2ORCID,Young Kaylene M1ORCID,Taylor Bruce V1

Affiliation:

1. Menzies Institute for Medical Research, University of Tasmania, Hobart, Tasmania, Australia

2. Sydney Neuroimaging Analysis Centre (SNAC), Sydney, New South Wales, Australia

3. School of Psychological Sciences, University of Tasmania, Hobart, Tasmania, Australia

4. School of Biological Sciences, The University of Western Australia, Crawley, Western Australia, Australia

5. Royal Hobart Hospital, Hobart, Tasmania, Australia

Abstract

Background Low-intensity repetitive transcranial magnetic stimulation (rTMS), delivered as a daily intermittent theta burst stimulation (iTBS) for four consecutive weeks, increased the number of new oligodendrocytes in the adult mouse brain. Therefore, rTMS holds potential as a remyelinating intervention for people with multiple sclerosis (MS). Objective Primarily to determine the safety and tolerability of our rTMS protocol in people with MS. Secondary objectives include feasibility, blinding and an exploration of changes in magnetic resonance imaging (MRI) metrics, patient-reported outcome measures (PROMs) and cognitive or motor performance. Methods A randomised (2:1), placebo controlled, single blind, parallel group, phase 1 trial of 20 rTMS sessions (600 iTBS pulses per hemisphere; 25% maximum stimulator output), delivered over 4–5 weeks. Twenty participants were randomly assigned to ‘sham’ ( n = 7) or active rTMS ( n = 13), with the coil positioned at 90° or 0°, respectively. Results Five adverse events (AEs) including one serious AE reported. None were related to treatment. Protocol compliance was high (85%) and blinding successful. Within participant MRI metrics, PROMs and cognitive or motor performance were unchanged over time. Conclusion Twenty sessions of rTMS is safe and well tolerated in a small group of people with MS. The study protocol and procedures are feasible. Improvement of sham is warranted before further investigating safety and efficacy.

Funder

Multiple Sclerosis Australia

National Health and Medical Research Council

Royal Hobart Hospital Research Foundation

Irene Phelps Charitable Trust

Medical Research Future Fund

Medical Protection Society of Tasmania

Publisher

SAGE Publications

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