Outcome measurement in functional neurological disorder: a systematic review and recommendations.
Susannah Pick, David G Anderson, Ali A Asadi-Pooya...
https://pubmed.ncbi.nlm.nih.gov/32111637Actively Recruiting
Led by Hospital Center Guillaume Régnier · Updated on 2026-04-20
22
Participants Needed
1
Research Sites
N/A
Total Duration
Functional neurological disorder (FND) causes significant suffering and disability through neurological symptoms that affect daily functioning without clear anatomical causes. This research focuses on motor symptoms like abnormal movements or motor deficits and aims to evaluate the impact of repetitive transcranial magnetic stimulation (rTMS) on patients' perceptions of improvement. The study also explores effects on symptoms from a clinician's viewpoint, quality of life, mood symptoms, dissociation, sense of agency, and rTMS side effects. Participants receive 40 sessions of intermittent theta burst rTMS targeting the right temporo-parietal junction (rTPJ) over 10 days, with four sessions per day. This non-invasive treatment uses magnetic pulses to modify brain activity and connectivity and is guided by neuronavigation. The protocol is based on recent research showing potential benefits and brain changes with this method in motor FND patients. During the study, patients' symptoms are assessed before and after treatment using patient and clinical global impression scales, movement disorder ratings, mood and fatigue scales, dissociation and agency measures, and quality of life surveys. Side effects are monitored throughout. The primary outcome is the change in patient global impression of change one month after treatment. The total evaluation period extends to about three months. This observational study aims to deepen understanding of rTMS effects on motor FND symptoms and patient well-being.
CONDITIONS
Impact of Theta Burst Repetitive Transcranial Magnetic Stimulation on the Patient's Self-reported Improvement in Their Motor Functional Neurological Disorder
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 10 days
Participants receive 40 sessions of intermittent theta burst repetitive transcranial magnetic stimulation (rTMS) targeting the right temporo-parietal junction (rTPJ) over 10 days.
4 sessions per day
Duration - 1 month and 3 weeks
Participants are monitored to assess the impact of rTMS treatment on their symptoms and quality of life, including patient and physician impression of change and side effects.
Visits occur during this period for assessments
Total: 1 location
1
Centre Hospitalier Guillaume Régnier
Rennes, France, 35000
Actively Recruiting
D
Dominique DRAPIER, PHD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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