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rTMS Effect in Functional Psychogenic Movement Disorders Applied Alone Then Combined With Hypnotherapy (MOVHYSTIM)

T

Toulouse University Hospital

Status

Completed

Conditions

Movement Disorders

Treatments

Device: rTMS

Study type

Interventional

Funder types

Other

Identifiers

NCT02471066
14 7311 02

Details and patient eligibility

About

The management of functional psychogenic movement disorders (FNPMD) is challenging for neurologists and psychiatrists and only comprehensive multidisciplinary treatment programme can be worthwhile for these patients (Moene et al 2002). Recent functional magnetic resonance imaging studies have demonstrated abnormalities in motor control at cortical level, hyperactivity of limbic system and disturbance of connectivity between these two systems leading to a lack of self-agency, (Voon et al 2010,2011).Two recent studies suggested a possible therapeutic effect of transcranial magnetic stimulation (TMS) in FNPMD (Dakotakis 2011, Garcin, 2013).

In this protocol our objectives are twofold :

  1. to compare the effect of 5 consecutive daily sessions of rTMS on FNPMD in a double-blind randomized controlled study
  2. to study the effect of 3 weekly hypnosis sessions combined with rTMS in FNPMD

Enrollment

18 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Man or woman with FNPMD for at least 2 months,
  • diagnosed from clinical Diagnostic and Statistical Manual V conversive somatoform troubles and Gupta & Lang (2009) and Edwards & Bahtia 2012 neurological clinical criteria

Exclusion criteria

  • Severe progressive psychiatric disorders
  • Cardiac pace-maker
  • Metallic prosthesis
  • Cochlear implants
  • Previous neurosurgery
  • Epilepsy
  • Severe cardiac disease
  • Alcohol or toxic abuse for the last 12 months
  • Drugs such clozapine, bupropion, methadone or theophylline

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

18 participants in 2 patient groups

active rTMS
Experimental group
Description:
12 patients will be enrolled in this arm.
Treatment:
Device: rTMS
sham rTMS
Sham Comparator group
Description:
12 patients will be enrolled in this arm.
Treatment:
Device: rTMS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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