Skip to content

A feasibility study of magnetic stimulation (using TMS - Transcranial Magnetic Stimulation) of the brain to improve limb weakness in motor conversion (functional neurological) disorder disorder

Trial Of Neurostimulation In Conversion Symptoms (TONICS) feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN51225587
Enrollment
20
Registered
2017-10-02
Start date
2017-10-03
Completion date
Unknown
Last updated
2020-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Motor conversion (functional neurological) disorder Nervous System Diseases Motor conversion (functional neurological) disorder

Interventions

Participants are initially provided with a detailed information sheet and have time to consider participation and to ask questions. Once a patient has provided written informed consent, they attend an

Sponsors

King's College London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. DSM5 diagnosis of motor conversion disorder made by consultant neurologist and/or neuropsychiatrist, causing weakness of at least one limb 2. Age =18 years 3. Ability to give written informed consent

Exclusion criteria

Exclusion criteria: 1. Epilepsy (or considered high risk of epilepsy from medical history) 2. Other contraindication to TMS (e.g. cochlear implants, metallic intracranial clips or intracranial surgery in last 12 months) 3. Comorbid organic neurological condition 4. Pain as primary symptom 5. Previous treatment with TMS (for any condition) 6. Non-fluent English speakers (if unable to accurately complete self-report questionnaires). 7. Major mental health disorder: current +/- previous diagnosis of schizophrenia or bipolar disorder; current drug/alcohol dependence 8. History of factitious disorder 9. Currently involved in another trial

Design outcomes

Primary

MeasureTime frame
Patient reported changes in symptoms measured using the patient-rated Clinical Global Impression of Improvement scale (CGI-I) at TMS session 1, TMS session 2 and at follow-up.

Secondary

MeasureTime frame
1. Assessor-rated symptom change measured using clinician-rated Clinical Global Impression of Improvement scale (CGI-I) at TMS session 1, TMS session 2 and follow-up 2. Disability and activities of daily living measured using functional rating scales: SF-36, Barthel, FIM/FAM at TMS session 1, TMS session 2 and follow-up 3. Current symptom severity measured using objective and subjective measures of strength: dynamometry and patient ratings at TMS session 1, TMS session 2 and follow-up 4. Current psychological symptoms measured using self-report questionnaires: GAD7, PHQ9, PHQ15 and CORE-10 at TMS session 1, TMS session 2 and at follow-up 5. Psychosocial outcomes measured with a self-report questionnaire: Work and Social Adjustment Scale at TMS session 1, TMS session 2 and at follow-up 6. Health economics measured using the Client Service Receipt Inventory at TMS session 1, TMS session 2 and at follow-up

Countries

United Kingdom

Contacts

Public ContactTim Nicholson
timothy.nicholson@kcl.ac.uk+44 207 848 5136

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 25, 2026