Transcranial Magnetic Stimulation (rTMS) and Autism.

NCT ID: NCT01648868

Last Updated: 2025-09-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

97 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-04-06

Study Completion Date

2019-05-13

Brief Summary

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In this protocol we aim to use rTMS to better characterize STS role in normal and abnormal social cognition. With that purpose, we will measure the effect of inhibitory and excitatory rTMS on the fixation time on social scenes (using eye-tracking methodology) or on the ability to recognize human voice/sounds.

Detailed Description

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Autism is characterized by severe impairments in verbal and non verbal communication and in social interactions. Results from cerebral imaging studies have suggested that abnormalities located on the superior temporal Sulcus (STS) level would be implicated in social impairments in autism. This abnormalities are both anatomical and functional: 1) rest hypoperfusion detected by positron emission tomography (PET); 2) abnormal activation during social tasks (fMRI) and 3) structural abnormalities shown on anatomical MRI. The STS is implicated in social cognition in normal subjects. Our hypothesis is that these anatomo-functional abnormalities would appear very early in brain development and could be one of the first steps in the cascade of neuronal dysfunction in autism. Transcranial Magnetic Stimulation (rTMS) is a technique which is used in cognitive neuroscience research as well as in therapeutic approaches in certain neurological and psychiatry diseases. It consists on applying a magnetic impulse on the brain trough the scalp in a non-invasive and painless by placing a coil on the surface of the head. This magnetic fields induce an electrical field which modifies activity of those neurons inside the magnetic field and induce an electrophysiological change in the target area. This process allows a non-invasive interaction with the human brain in action during focal stimulations. In cognitive neuroscience research, we are interested in the modifications caused by rTMS in cognitive performances in order to better precise the functional role of the target region. The intensity and the frequency of the impulse can be controlled (frequency \<1 Hz = inhibitory effect ; frequency \> 3 Hz = excitatory effect). The functional characteristics of a given region and it's eventual dysfunctions may be identified thank to the abnormalities in reactivity and cortical connectivity. The goal of this project is to study inhibitory and excitatory effects of rTMS applied to the STS in healthy controls and patients with autism. This effect will be measured by two main parameters of social cognition: 1) visual perception of social scenes, measured by eye-tracking methodology; 2) auditory perception of human voice. We will study 50 healthy voluntaries controls and 50 patients with a non-syndromic autism (18 to 25 years old; IQ \> 60), diagnosed by DSM-IV and ADI-R. All participants will undergo an structural MRI and a rTMS session on the STS. In both cases, the STS will be localised based on the structural MRI. The total duration of the rTMS session is about two hours. All data will be analysed by the adapted statistical methods. This study will allow a better understanding of the role of STS in social cognition in healthy subjects as well as it's implication in the social impairments which characterize autism. Finally, the rTMS may become, in a near future, a innovative therapeutic strategy in autism.

Conditions

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Autism Spectrum Disorder

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Excitatory effects of rTMS

Study excitatory effects of rTMS applied to the STS in patients with autism

Group Type EXPERIMENTAL

Transcranial Magnetic Stimulation (rTMS)

Intervention Type DEVICE

Excitatory effects of Transcranial Magnetic Stimulation (rTMS) applied to the STS in patients with autism.

Inhibitory effects of rTMS

Study inhibitory effects of rTMS applied to the STS in healthy controls

Group Type ACTIVE_COMPARATOR

Transcranial Magnetic Stimulation (rTMS)

Intervention Type DEVICE

Inhibitory effects of Transcranial Magnetic Stimulation (rTMS) applied to the STS in healthy controls

Interventions

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Transcranial Magnetic Stimulation (rTMS)

Excitatory effects of Transcranial Magnetic Stimulation (rTMS) applied to the STS in patients with autism.

Intervention Type DEVICE

Transcranial Magnetic Stimulation (rTMS)

Inhibitory effects of Transcranial Magnetic Stimulation (rTMS) applied to the STS in healthy controls

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

Patients with autism

* Age from 18 to 30 years old
* Autism diagnosed by DSM-IV and ADI-R
* IQ \> 60 or able to have an MRI
* Social security registration
* Consent form signed by patient or legal tutor

Healthy controls

* Age from 18 to 30 years old
* Medical exam previous to the interventions
* Social security registration
* Consent form signed

Exclusion Criteria

All Patients

* Indication against MRI (pace-maker, metallic pieces in the body, working with metals)
* Indications against rTMS (epilepsy, epilepsy family history, craniotomy scarf, pace maker or neuron stimulator, intraocular or intra-cerebral strange metallic piece, cochlear implant, cardiac valve, chirurgical metallic arterial material, metallic material susceptible to concentrate radio-frequency impulse)
* Claustrophobia
* Pregnant woman
* Women in a fertile age with no efficient contraception method
* Use of drugs diminishing cortical excitability
* Participation in another clinical trial that forbids the participation in this one
* Have already being treated by some electrical or magnetic stimulation technique ( transcutaneous or radicular stimulation)
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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URC-CIC Paris Descartes Necker Cochin

OTHER

Sponsor Role collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nathalie BODDAERT, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Necker-Enfants Malades Hospital

Monica ZILBOVICIUS, PhD

Role: STUDY_DIRECTOR

Institut National de la Santé Et de la Recherche Médicale, France

Locations

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Hôpital Necker-Enfants Malades

Paris, , France

Site Status

Countries

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France

References

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Saitovitch A, Popa T, Lemaitre H, Rechtman E, Lamy JC, Grevent D, Calmon R, Meunier S, Brunelle F, Samson Y, Boddaert N, Zilbovicius M. Tuning Eye-Gaze Perception by Transitory STS Inhibition. Cereb Cortex. 2016 Jun;26(6):2823-31. doi: 10.1093/cercor/bhw045. Epub 2016 Mar 5.

Reference Type BACKGROUND
PMID: 26946130 (View on PubMed)

Saitovitch A, Lemaitre H, Rechtman E, Vincon-Leite A, Calmon R, Grevent D, Dangouloff-Ros V, Brunelle F, Boddaert N, Zilbovicius M. Neural and behavioral signature of human social perception. Sci Rep. 2019 Jun 25;9(1):9252. doi: 10.1038/s41598-019-44977-8.

Reference Type BACKGROUND
PMID: 31239453 (View on PubMed)

Other Identifiers

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2009-A01025-52

Identifier Type: REGISTRY

Identifier Source: secondary_id

P081232

Identifier Type: -

Identifier Source: org_study_id

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