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Clinical Trials/NCT06645587
NCT06645587
Recruiting
Not Applicable

Understanding and Targeting Repetitive Behaviors and Restricted Interests in Autism Spectrum Disorder Via High-Definition Transcranial Direct Current Stimulation

Bambino Gesù Hospital and Research Institute1 site in 1 country78 target enrollmentOctober 3, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Autism Spectrum Disorder
Sponsor
Bambino Gesù Hospital and Research Institute
Enrollment
78
Locations
1
Primary Endpoint
Repetitive Behavior Scale-Revised
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

Repetitive behaviors (RBs) are a prevalent feature of Autism Spectrum Disorder (ASD). There are two groups of RBs: lower-order (e.g. motor stereotypies) and higher-order RBs (e.g. restricted interests), linked to sensory-motor and the associative loops, respectively. To date, treatment options for RBs are very limited. High-definition transcranial direct current stimulation (HD-tDCS) may be effective in reducing the impact of RBs in children with ASD by targeting the associated brain alterations. Moreover, the high focality of HD-tDCS will help the investigators to disentangle the relative contribution of different brain loops (namely, sensory-motor and the associative loops) into RBs subtypes. The investigators will also study the electrophysiological patterns associated to behavioral changes after the application of HD-tDCS.

Detailed Description

The experimental design will be the following: randomized, three-arm, between subject, double blind, and placebo-controlled. Children and adolescents with ASD will be selected and randomly assigned to three groups: 1. Active high-definition tDCS (HD-tDCS) over pre-SMA; 2. Active high-definition tDCS (HD-tDCS) left DLPFC; 3. Sham high-definition tDCS (HD-tDCS). In this project, the investigators will work to understand whether a brain-based intervention, with the use of HD-tDCS can enhance RBs in individuals with ASD. The protocol will allow the investigators to: 1. Test if Active high-definition tDCS (HD-tDCS) compared to sham HD-tDCS will contribute in reducing RBs 2. Test if HD-tDCS over pre-SMA cortex will decrease lower-order RBs, while HD-tDCS over dlPFC will decrease higher-order RBs 3. Test if the Active Groups will significantly improve in the remaining psychological measures compared to the Sham Group 4. Test if the Active Groups will change in the RBS-R total score will be significantly correlated with changes in neuropsychological and electroencephalographic (EEG) connectivity measures 5. Test if the Active Groups will change in the RBS-R total score will be significantly correlated with changes in the remaining psychological measures and parental stress. The overarching goal is to provide a scientific foundation for devising new rehabilitation strategies in ASD.

Registry
clinicaltrials.gov
Start Date
October 3, 2024
End Date
April 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Bambino Gesù Hospital and Research Institute
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • participants of both genders with ASD diagnosis according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) and based on clinical evaluation and administration of gold standard tools for ASD diagnosis
  • an intelligence quotient (IQ) higher or equal to 70 (IQ ≥ 70)
  • age range from 8 years to 13 years and 11 months included

Exclusion Criteria

  • the presence of neurological/medical/genetic conditions (i.e., brain tumours or genetic syndromes)
  • personal or family history of epilepsy
  • other primary psychiatric diagnoses (i.e., bipolar disorders, schizophrenia spectrum disorders, or adjustment disorder)
  • sensorimotor deficits
  • the presence of peacemaker or other metal devices in the body;
  • ongoing CNS-active drug treatment
  • receiving other cognitive-behavioral therapies specifically focused on RBs in the 3 months before the study

Outcomes

Primary Outcomes

Repetitive Behavior Scale-Revised

Time Frame: Baseline, pre-intervention; immediately after the intervention; three-month follow-up.

The primary outcome measure will be the Total Score of the Repetitive Behavior Scale-Revised (Bodfish, 2000). It consists of a 43-item parent-report questionnaire evaluating the extent of RBs in individuals with ASD. The tool encompasses six scales: Stereotyped Behavior (6 items), Self-injurious Behavior (8 items), Compulsive Behavior (8 items), Routine Behavior (6 items), Sameness Behavior (11 items), and Restricted Behavior (4 items). The items are rated on a four-point scale (0-Behavior does not occur, 1-Behavior occurs and is a mild problem, 2-Behavior occurs and is a moderate problem, 3-Behavior occurs and is a severe problem); an overall total raw score and a total number of items score for each subscale are computed. Higher scores indicate greater severity of repetitive behaviors. The sum of all items provides a total raw score ranging from 0 to 129, with higher scores indicating more severe repetitive behaviors.

Secondary Outcomes

  • Wisconsin Card Sorting Test(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Stop Signal Task(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Short Sensory Profile 2(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Behavior Rating Inventory of Executive Function - Second Edition/ parent report(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Sleep Disturbance Scale for Children(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Child Behaviour Checklis/ 6-18(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Childhood Autism Rating Scale-2(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Parenting Stress Index Short Form(Baseline, pre-intervention; immediately after the intervention; three-month follow-up.)
  • Electroencephalography (HD-EEG)(Baseline, pre-intervention and immediately after the intervention.)

Study Sites (1)

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