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Modulation of the Activity of the Cerebellum in Autism (MACA) (MACA)

Primary Purpose

Autism Spectrum Disorder

Status
Recruiting
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
tDCS
Sponsored by
Beatriz Catoira
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Autism Spectrum Disorder focused on measuring tDCS, Cerebellum, neuromodulation, autism

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Participant Inclusion/exclusion criteria: Participants must be more than 18 years old normal eyesight and hearing; Dutch, French or English speaking; Neurotypical participants inclusion/exclusion criteria: No disorder (now or in the past) that could have affected the brain such as cerebrovascular accidents (CVA), neurodegenerative disorders, or essential tremor; No neurological diseases that could affect reasoning or intellectual abilities (such as Parkinson's Disease, Epilepsy, and Multiple Sclerosis) Neurotypical participants will be matched on age and gender to the ASD population; ASD participants inclusion/exclusion criteria: Patients with a formal diagnosis of high-functioning ASD as determined by the clinical psychologist/psychiatrist.

Sites / Locations

  • UZ BrusselRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Active Comparator

Sham Comparator

Active Comparator

Sham Comparator

Active Comparator

Sham Comparator

Arm Label

ASD_anodalstimulation

ASD_shamstimulation

NT_anodalstimulation

NT_shamstimulation

H-AQ_anodalstimulation

H-AQ_shamstimulation

Arm Description

ASD participant, anodal stimulation on the first session, sham stimulation on the second sesion

ASD participant, sham stimulation on the first session, anodal stimulation on the second sesion

Neurotypical participant, anodal stimulation on the first session, sham stimulation on the second sesion

Neurotypical participant, sham stimulation on the first session, anodal stimulation on the second sesion

non diagnosed autistic participant,anodal stimulation on the first session, sham stimulation on the second sesion

non diagnosed autistic participant, sham stimulation on the first session, anodal stimulation on the second sesion

Outcomes

Primary Outcome Measures

PS_RT
Reaction Time in the pictorial sequencing time
PS_accuracy
Accuracy in the pictorial sequencing task
ER_RT
Reaction Times in the emotion recognition task
ER_accuracy
Accuracy in the emotion recognition task
Brain activity at the emotion recognition task
Brain activity (fMRI) in regions of interest/whole brain analysis. Differences between stimulation and sham, between task conditions and between sessions as well as possible interactions in between those factors and covariates (AQ scores, age, gender...)
Brain activity at resting state
Brain activity (fMRI) in regions of interest/whole brain analysis. Differences between stimulation and sham, between task conditions and between sessions as well as possible interactions in between those factors and covariates (AQ scores, age, gender...)
Brain activity at the pictorial sequencing task
Brain activity (fMRI) in regions of interest/whole brain analysis. Differences between stimulation and sham, between task conditions and between sessions as well as possible interactions in between those factors and covariates (AQ scores, age, gender...)
White matter integrity in the cerebellum
White matter integrity matrix (FA, MD, RD) in the cerebellum using tract-based spatial statistics in the cerebellum & differences between groups

Secondary Outcome Measures

Connectivity_PStask
Brain connectivity (fMRI) analysis on the pictorial sequencing task
Connectivity_ERtask
Brain connectivity (fMRI) analysis on the emotion recognition task
Connectivity_stimulation
Brain connectivity (fMRI) analysis during stimulation
Fiber tractography between the cerebellum and the default mode/ mentalizing network
Fiber tractography (Diffusion weighted imaging) between the cerebellum and the default mode / mentalizing network, by extraction of white matter integrity parameters on each fiber tract
ROI-based structural connectivity
Structural connectivity (DWI) between ROIs from the default mode/mentalizing network
Whole brain structural network construction
Structural connectivity (DWI) within the whole brain using graph theory

Full Information

First Posted
December 6, 2022
Last Updated
April 4, 2023
Sponsor
Beatriz Catoira
Collaborators
Vrije Universiteit Brussel, University Ghent, Universitair Ziekenhuis Brussel
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1. Study Identification

Unique Protocol Identification Number
NCT05781412
Brief Title
Modulation of the Activity of the Cerebellum in Autism (MACA)
Acronym
MACA
Official Title
Modulation of the Activity in the Cerebellum With Transcranial Direct Current Stimulation in Autistic Participants
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 24, 2022 (Actual)
Primary Completion Date
March 1, 2024 (Anticipated)
Study Completion Date
October 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Beatriz Catoira
Collaborators
Vrije Universiteit Brussel, University Ghent, Universitair Ziekenhuis Brussel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Research on the involvement of the cerebellum in social understanding behavior and the mentalizing brain system has just begun. Knowledge about the neurobiology of social understanding is important for understanding the ways to manipulate these processes. Like cerebral tDCS, cerebellar tDCS could then be used to enhance more complex processes, such as mentalizing, in healthy individuals. It can eventually also be examined as a therapeutic tool for patients with mentalizing difficulties such as patients with ASD. In this study, it is examined whether anodal tDCS at the right posterior cerebellum influences social understanding and which cerebro-cerebellar networks play a role in this process.
Detailed Description
Autism Spectrum Disorders (ASD) are a group of lifelong neurodevelopmental disorders characterized by social and communicative difficulties and repetitive and stereotyped behaviors. Research has shown that cerebellar abnormalities are among the most important etiological factors for ASD. The cerebellum is found to be most frequently involved in tasks where participants must remember or imagine past or future autobiographical events, judge persons or situations based on behavioral sentences, make trait inferences of others using stories, words or faces, and describe persons or objects based on behavioral or object pictures. Recent research has also provided evidence on the involvement of the posterior areas of the cerebellum in social cognition. Specifically, the areas crus I and crus II, located at the lateral hemispheres of the posterior cerebellum, are associated with more complex cognitive and social processes, such as mentalizing. Mentalizing is the cognitive ability to attribute mental states, such as desires, intentions, and beliefs, to other people. This ability is needed to understand and predict other people's behavior and is the main component of social cognition. Problems with mentalizing, including the attribution of false beliefs to others, are characteristic for autism spectrum disorder (ASD). A sequencing task (that included social and non social conditions) showing that cerebellar patients performed worse than healthy participants. Facial emotion recognition refers to the ability to derive emotional meaning from facial expressions and has been shown to underlie social competency. Recent literature reviews have reported significant facial emotion recognition impairments in individuals with ASD. These impairments take various forms, such as a reduced accuracy in labeling facial emotions or reduced specificity in rating facial emotions of varying intensity . Thus, there is evidence suggesting that ASD is associated with a selective impairment in facial emotion recognition. Transcranial direct current stimulation (tDCS) is a noninvasive technique that can produce long-lasting changes in the excitability and spontaneous activity of the stimulated brain areas. Therefore, tDCS is investigated as a possible treatment for different psychiatric diseases. Cerebellar tDCS have shown to also produce prolonged changes successfully at the neural and behavioral level. However, due to the high density of neurons in the cerebellum and diffuse connections to the cerebrum, it is more difficult to understand the working mechanisms of cerebellar as compared to cerebral tDCS. In addition, the electrical current will spread across more neurons in the cerebellum by cerebellar tDCS and will functionally affect the cerebral regions to which these cerebellar neurons are connected as well. Therefore, the type of behavioral effect, such as an improvement of performance after anodal tDCS or an impairment of performance after cathodal tDCS, is harder to predict for cerebellar than cerebral tDCS. Modulation of social understanding with tDCS has been studied by stimulating the key mentalizing regions mPFC and TPJ. In healthy participants, an improvement on tasks was found that required the enhancement or inhibition of representation of the self or of others, which is important for mentalizing, after anodal tDCS at the TPJ compared to sham tDCS or cathodal tDCS. The effect of cerebellar tDCS on social understanding using action sequences has not yet been examined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder
Keywords
tDCS, Cerebellum, neuromodulation, autism

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
There will be three groups of participants: autism-diagnosed, autism-non-diagnosed and neurotypical individuals (healthy controls). On each group, participants will be randomly allocated to one of two groups: anodal stimulation in the first session or anodal stimulation in the second session (in the other session there will be sham stimulation).
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ASD_anodalstimulation
Arm Type
Active Comparator
Arm Description
ASD participant, anodal stimulation on the first session, sham stimulation on the second sesion
Arm Title
ASD_shamstimulation
Arm Type
Sham Comparator
Arm Description
ASD participant, sham stimulation on the first session, anodal stimulation on the second sesion
Arm Title
NT_anodalstimulation
Arm Type
Active Comparator
Arm Description
Neurotypical participant, anodal stimulation on the first session, sham stimulation on the second sesion
Arm Title
NT_shamstimulation
Arm Type
Sham Comparator
Arm Description
Neurotypical participant, sham stimulation on the first session, anodal stimulation on the second sesion
Arm Title
H-AQ_anodalstimulation
Arm Type
Active Comparator
Arm Description
non diagnosed autistic participant,anodal stimulation on the first session, sham stimulation on the second sesion
Arm Title
H-AQ_shamstimulation
Arm Type
Sham Comparator
Arm Description
non diagnosed autistic participant, sham stimulation on the first session, anodal stimulation on the second sesion
Intervention Type
Device
Intervention Name(s)
tDCS
Intervention Description
Anodal and Sham cerebellar tDCS will be used in each participant in a counterbalanced order
Primary Outcome Measure Information:
Title
PS_RT
Description
Reaction Time in the pictorial sequencing time
Time Frame
assessment will begin 10 minutes after stimulation and last up to 15 minutes
Title
PS_accuracy
Description
Accuracy in the pictorial sequencing task
Time Frame
assessment will begin 10 minutes after stimulation and last up to 15 minutes
Title
ER_RT
Description
Reaction Times in the emotion recognition task
Time Frame
assessment will begin 20 minutes after stimulation and last up to 5 minutes
Title
ER_accuracy
Description
Accuracy in the emotion recognition task
Time Frame
assessment will begin 20 minutes after stimulation and last up to 5 minutes
Title
Brain activity at the emotion recognition task
Description
Brain activity (fMRI) in regions of interest/whole brain analysis. Differences between stimulation and sham, between task conditions and between sessions as well as possible interactions in between those factors and covariates (AQ scores, age, gender...)
Time Frame
assessment will begin 20 minutes after stimulation and last up to 5 minutes
Title
Brain activity at resting state
Description
Brain activity (fMRI) in regions of interest/whole brain analysis. Differences between stimulation and sham, between task conditions and between sessions as well as possible interactions in between those factors and covariates (AQ scores, age, gender...)
Time Frame
assesment will begin concurrent with stimulation and last up to 20 minutes
Title
Brain activity at the pictorial sequencing task
Description
Brain activity (fMRI) in regions of interest/whole brain analysis. Differences between stimulation and sham, between task conditions and between sessions as well as possible interactions in between those factors and covariates (AQ scores, age, gender...)
Time Frame
assessment will begin 10 minutes after stimulation and last up to 15 minutes
Title
White matter integrity in the cerebellum
Description
White matter integrity matrix (FA, MD, RD) in the cerebellum using tract-based spatial statistics in the cerebellum & differences between groups
Time Frame
assessment will begin immediately after stimulation and last up to 10 minutes
Secondary Outcome Measure Information:
Title
Connectivity_PStask
Description
Brain connectivity (fMRI) analysis on the pictorial sequencing task
Time Frame
assessment will begin 10 minutes after stimulation and last up to 15 minutes
Title
Connectivity_ERtask
Description
Brain connectivity (fMRI) analysis on the emotion recognition task
Time Frame
assessment will begin 20 minutes after stimulation and last up to 5 minutes
Title
Connectivity_stimulation
Description
Brain connectivity (fMRI) analysis during stimulation
Time Frame
assesment will begin concurrent with stimulation and last up to 20 minutes
Title
Fiber tractography between the cerebellum and the default mode/ mentalizing network
Description
Fiber tractography (Diffusion weighted imaging) between the cerebellum and the default mode / mentalizing network, by extraction of white matter integrity parameters on each fiber tract
Time Frame
assessment will begin immediately after stimulation and last up to 10 minutes
Title
ROI-based structural connectivity
Description
Structural connectivity (DWI) between ROIs from the default mode/mentalizing network
Time Frame
assessment will begin immediately after stimulation and last up to 10 minutes
Title
Whole brain structural network construction
Description
Structural connectivity (DWI) within the whole brain using graph theory
Time Frame
assessment will begin immediately after stimulation and last up to 10 minutes
Other Pre-specified Outcome Measures:
Title
Electrical Field Simulations
Description
Simulation of the electric field generated by the tDCS stimulation.
Time Frame
First 10 minutes of assessment
Title
Correlations between DWI, behavioural data, simulation and functional data
Description
The primary outcome measures from the diffusion weighted imaging will provide different measures for structural connectivity per participant. The correlation of these measures with behavioural and/or functional data will be computed.
Time Frame
assessment will include data from the 60 minutes that are spent in the scanner in the session

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Participant Inclusion/exclusion criteria: Participants must be more than 18 years old normal eyesight and hearing; Dutch, French or English speaking; Neurotypical participants inclusion/exclusion criteria: No disorder (now or in the past) that could have affected the brain such as cerebrovascular accidents (CVA), neurodegenerative disorders, or essential tremor; No neurological diseases that could affect reasoning or intellectual abilities (such as Parkinson's Disease, Epilepsy, and Multiple Sclerosis) Neurotypical participants will be matched on age and gender to the ASD population; ASD participants inclusion/exclusion criteria: Patients with a formal diagnosis of high-functioning ASD as determined by the clinical psychologist/psychiatrist.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Beatriz Catoira, Msc
Phone
+32456267472
Email
Beatriz.catoira@vub.be
First Name & Middle Initial & Last Name or Official Title & Degree
Nathalie Vanderbruggen
Phone
02/ 4763599
Email
Nathalie.Vanderbruggen@uzbrussel.be
Facility Information:
Facility Name
UZ Brussel
City
Jette
State/Province
Brussels
ZIP/Postal Code
1090
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Beatriz Catoira
Phone
0456267472
Ext
0032
Email
beatriz.catoira@vub.be

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Modulation of the Activity of the Cerebellum in Autism (MACA)

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