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Intermittent Theta-Burst Stimulation to Target Irritability in Adults With ASD

Intermittent Theta-Burst Stimulation to Target Irritability in Adults With ASD

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04316338
Enrollment
0
Registered
2020-03-20
Start date
2022-05-01
Completion date
2025-05-01
Last updated
2023-11-28

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

Conditions

Autism Spectrum Disorder

Brief summary

This study aims to demonstrate the feasibility, tolerability, safety and preliminary efficacy of 6 weeks of fMRI-guided iTBS delivered to personalized regions of the prefrontal cortex (PFC) in adults with ASD in reducing irritability in adults with ASD.

Interventions

Non-invasive brain stimulation technique

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Open-label design.

Eligibility

Sex/Gender
ALL
Age
22 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of ASD or Asperger's based on DSM-5 criteria as confirmed by a qualified clinician (including Dr. Fung), and if necessary the administration of Autism Diagnostic Interview-Revised (ADI-R) and/or Autism Diagnostic Observation Schedule-Generic (ADOS-G) 2. Age 22 to 55. 3. Adults who are physically healthy. 4. No significant current psychosocial stressors per history. 5. Full scale IQ \> 50. 6. ABC-I score of 18 or greater. 7. if the participant is taking medication, they must be stable on this medication regiment for at least 4 weeks prior to baseline and agree to stay on these medications for the duration of the trial

Exclusion criteria

(f) Pre-term birth (\<34 weeks' gestation) (g) Low birth weight (\<2000 g). (h) DSM-5 diagnosis of other severe psychiatric disorder such as bipolar disorder or schizophrenia. (i) Current use of benzodiazepines. (j) Use of other medications that modulate the GABA(A) receptor within 4 weeks of scanning (8 weeks for fluoxetine). (k) History of alcoholism or substance abuse. (l) Active medical problems such as unstable seizures, congenital heart disease, endocrine disorders. (m) Significant sensory impairments such as blindness or deafness. (n) Contraindication for MRI. (o) Pregnancy. (p) evidence of genetic syndrome.

Design outcomes

Primary

MeasureTime frameDescription
Aberrant Behavior Checklist-irritability subscale (ABC-I)Change across time: Baseline minus immediately after final treatmentA parent/caregiver/clinician completed checklist (58-item) with an irritability subscale (15-item). Each item has a maximum score of 3, meaning that the irritability subscale has a maximum score of 45 and minimum score of 0. Higher scores indicate higher levels of irritability.

Secondary

MeasureTime frameDescription
Self-injury questionnaire (SIQ)Baseline, immediately after treatment, one month after treatment.Self-report measure of self-injury, maximum 60 questions but participants only answer relevant questions. Five types of self-injurious behaviors are checked: scratching, bruising, cutting, burning, and biting oneself. It will assess the taxonomic specifications of self-injurious behavior (SIB- (e.g., type, frequency, duration)), but also the affective antecedents and consequences as well as the functions of each type of SIB.
THE MODIFIED OVERT AGGRESSION SCALE (MOAS)Baseline, immediately after treatment, one month after treatment.Clinician rated scale of aggression. 4 items rated from 0-4. Maximum score is 16 with higher scores indicating higher levels of aggression, used to evaluate and document the frequency and severity of aggressive episodes.
Difficulties in Emotion Regulation ScaleBaseline, immediately after treatment, one month after treatment.Self-report measure of emotion regulation, evaluating individuals' levels of difficulties in regulating emotions. 36-item questionnaires. Each question rated from 1-5. Maximum score is 180 with higher scores indicating greater difficulty in emotion regulation. The instrument presents 36 items on a 5-point Likert scale of frequency (from 1 = almost never, to 5 = almost always).
The Adult Autism Quotient (AQ)Baseline, immediately after treatment, one month after treatment.50-item self-report measure of autistic traits. Each of 50 statements are rated from 'definitely disagree' to 'definitely agree'.
Repetitive Behavior Scale-Revised (RBS-R)Baseline, immediately after treatment, one month after treatment.43-item clinician rated scale measuring repetitive behaviors associated with ASD. Each item is rated from 0 (behavior does not occur) to 3 (behavior is a severe problem)
Irritability QuestionnaireBaseline, every week of treatment (1-6), immediately after treatment, one month after treatment.A 21-item self-report measure of irritability. Each item is rated on how often (Never=0 to Most of the time=4) and the intensity (Not at all=0, Very much so=4) at which they occur.
Functional connectivity between areas involved in negative emotion regulationBaseline, immediately after treatment, one month after treatment.Functional magnetic resonance imaging (fMRI) will be used to measure functional connectivity between areas involved in emotion regulation, previously shown to be involved in irritability. Areas of interest include: ventromedial prefrontal cortex, the amygdala, dorsolateral prefrontal cortex, the striatum.
EEG recordingsBaseline, immediately after treatment, one month after treatment.Electroencephalography (EEG) will be used to measure brain activity and connectivity before and after treatment. Resting-state EEG (5 minutes) with eyes open and TMS-evoked potential recordings will be taken before and after treatment. We are particularly interested in measuring gamma band activity (\>30Hz) in participants while at rest.
Magnetic resonance spectroscopy (MRS)Baseline, immediately after treatment, one month after treatment.MRS will be used to measure GABA levels in two brain areas of interest (ventromedial prefrontal cortex and amygdala) before and after treatment.
Aberrant Behavior Checklist-irritability subscale (ABC-I)Change across time: Baseline minus one month after treatmentA parent/caregiver/clinician completed checklist (58-item) with an irritability subscale (15-item). Each item has a maximum score of 3, meaning that the irritability subscale has a maximum score of 45 and minimum score of 0. Higher scores indicate higher levels of irritability.
Montgomery-Åsberg Depression Rating Scale (MADRS)Baseline, immediately after treatment, one month after treatment.10-item clinician rated measure of depressive symptoms. Each item is rated on a scale of 1-6.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026