Enhancement of Behavioral and Cognitive Outcomes in Autism Spectrum Disorder Via Neurostimulation
Primary Purpose
Autism Spectrum Disorder
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Trans Cranial Magnetic Stimulation
Sponsored by
About this trial
This is an interventional treatment trial for Autism Spectrum Disorder
Eligibility Criteria
Inclusion criteria
- Fulfilling the Diagnostic and Statistical Manual for Mental Disorders 5th edition (DSM-V) criteria for ASD and confirmed by Gilliam Asperger Disorder Scale (GADS)
- The patient exhibiting adequate understanding and cooperation for the procedure
Exclusion criteria
- Patients with ASD exhibiting significant anxiety or contact avoidance, precluding them from cooperating with the procedure
- Children with a known diagnosis of seizures
- Presence of any metallic implants or devices in the head or neck area
- Pregnant women
Sites / Locations
- Mitra AssadiRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
left IPL stimulation
right IPL stimulation
Arm Description
half of the subjects will receive TMS on the left inferior parietal lobule.
half of the subjects will receive TMS on the right inferior parietal lobule.
Outcomes
Primary Outcome Measures
The effects of rTMS on reciprocal social cognition
The Social Responsiveness Scale - Second Edition (SRS-2) is a 65-item, parent/caregiver-rated scale assessing social interaction and communication deficits. . Raw scores range from 65 to 260 and higher scores suggest worse symptoms.
The effects of rTMS on reciprocal rigid patterns of behavior
Repetitive Behavior Scale-Revised is a parent rated scale that measures restricted repetitive behaviors. The total score is the sum of all 43 items and can range from 0 to 129.
Secondary Outcome Measures
The effect of rTMS on verbal fluency
The Delis-Kaplan Executive Function System (D-KEFS) Verbal Fluency task
The effects of rTMS on executive function
The Flanker Inhibitory Control and Attention is a test to measure the inhibitory and attentional facets of Executive Functioning
The effects of rTMS on executive function
The Dimensional Change Card Sort is a task designed to assess cognitive flexibility.
Full Information
NCT ID
NCT05371912
First Posted
May 1, 2022
Last Updated
May 10, 2022
Sponsor
Christiana Care Health Services
Collaborators
Dupont Applied Biosciences
1. Study Identification
Unique Protocol Identification Number
NCT05371912
Brief Title
Enhancement of Behavioral and Cognitive Outcomes in Autism Spectrum Disorder Via Neurostimulation
Official Title
Enhancement of Behavioral and Cognitive Outcomes in Autism Spectrum Disorder Via Neurostimulation
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 15, 2022 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Christiana Care Health Services
Collaborators
Dupont Applied Biosciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Autism spectrum disorder (ASD) encompasses a range of limitations in reciprocal social and communicative milestones, as well as restrictive and/or repetitive patterns of behavior which lead to significant functional challenges impacting individuals throughout their lifespan. There are major shortcomings in the existing pharmacological interventions; they are of limited efficacy, target a subset of problematic behaviors, and fail to improve social cognition. To overcome these limitations and improve outcomes, the investigators study the use of neurostimulation to mitigate the social and cognitive manifestations of ASD.
Detailed Description
Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive neurostimulation technique that alters cortical excitability by repeated induction of electromagnetic activity. FDA approved for depression, rTMS is a promising tool in the field of neuropsychiatry with an excellent safety profile. A prevailing hypothesis in ASD proposes that mirror neuron dysfunction in the inferior parietal lobule (IPL) contributes to the core deficits. The left and right IPL regions support different social and cognitive functions and moreover, are differentially impacted in ASD. Therefore, it can be expected that enhancing function of the IPL may produce positive but hemispheric-dependent effects on social cognition. The investigators long-term goal in this pilot proposal is to understand whether stimulating IPL with rTMS improves social and cognitive outcomes in ASD.
This research, which builds upon our proof-of-concept testing of 4 patients, proposes 10 sessions of rTMS stimulation of the IPL. Participants will be randomized to receive active stimulation to either the left or right-IPL (with sham stimulation to the contralateral side) in a prospective, double-blind protocol during which neither the subject nor the neuropsychologist obtaining and interpreting the outcome measures will have awareness of the rTMS group. For targeting the IPL, which correlates with the Brodmann areas 40/7 on the cortex, the investigators use disposable mapping caps, and for the purpose of blinding, the investigators use a standard shamming technique. Outcome measures include neuropsychological testing administered at baseline, after completion of TMS regime, and three months later. Within this design, the investigators have three aims:
Aim 1: Assess the differential effects of rTMS of the left versus right IPL on linguistic abilities and executive function in ASD. Hypothesis: rTMS stimulation of the IPL leads to long term potentiation and hence enhances cognitive performance in a hemispheric dependent manner with left-IPL stimulation enhancing linguistic ability and right-IPL stimulation enhancing executive function. To measure the effects, the investigators will use the Delis-Kaplan Executive Function System Verbal Fluency task (D-KEFS) and two elements of the NIH toolbox: Flanker: a test to measure the inhibitory and attentional facets of Executive Functioning. Dimensional Change Card Sort (DCCS): a task designed to assess cognitive flexibility. The investigators expect improvement in the Flanker and DCCS scores with right IPL stimulation and D-KEFS score improvement with left IPL stimulation.
Aim 2: Determine the effects of unilateral rTMS of the IPL on social/behavioral deficits in children and young adults with ASD. Hypothesis: rTMS simulation of the mirror neuron system potentiates similar improve-ments in social cognition despite hemispheric laterality via separate but related mechanisms. To measure the outcomes of right v/s left unilateral IPL stimulation, the investigators will use two standard scales and compare the numerical values before and after the intervention. The Social Responsiveness Scale - 2nd Edition (SRS2) and the Repetitive Behavior Scale-Revised (RRBs) are validated parent/caregiver-rated scale of social/communication deficits and restricted/repetitive behaviors respectively.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The patients will be randomized at the time of recruitment to either receiving left or right IPL stimulation. A shamming technique will be applied to the opposite hemisphere. Both the patient and the neuropsychologist obtaining and interpreting the outcome measures will be blinded regarding the hemispheric side of rTMS intervention. Only the clinician delivering the rTMS treatment will have a knowledge about the treatment targeting.
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
The TMS coil will be placed on the scalp at a 90 degree angle and will be turned on to create the perception of delivering the stimulation to the brain.
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
left IPL stimulation
Arm Type
Active Comparator
Arm Description
half of the subjects will receive TMS on the left inferior parietal lobule.
Arm Title
right IPL stimulation
Arm Type
Active Comparator
Arm Description
half of the subjects will receive TMS on the right inferior parietal lobule.
Intervention Type
Device
Intervention Name(s)
Trans Cranial Magnetic Stimulation
Intervention Description
Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive neurostimulation technique that alters cortical excitability by repeated induction of electromagnetic activity. FDA approved for depression, rTMS is a promising tool in the field of neuropsychiatry with an excellent safety profile.
Primary Outcome Measure Information:
Title
The effects of rTMS on reciprocal social cognition
Description
The Social Responsiveness Scale - Second Edition (SRS-2) is a 65-item, parent/caregiver-rated scale assessing social interaction and communication deficits. . Raw scores range from 65 to 260 and higher scores suggest worse symptoms.
Time Frame
to demonstrate a change produced by 5 weeks of rTMS
Title
The effects of rTMS on reciprocal rigid patterns of behavior
Description
Repetitive Behavior Scale-Revised is a parent rated scale that measures restricted repetitive behaviors. The total score is the sum of all 43 items and can range from 0 to 129.
Time Frame
to demonstrate a change produced by 5 weeks of rTMS
Secondary Outcome Measure Information:
Title
The effect of rTMS on verbal fluency
Description
The Delis-Kaplan Executive Function System (D-KEFS) Verbal Fluency task
Time Frame
at baseline and 5 weeks of rTMS
Title
The effects of rTMS on executive function
Description
The Flanker Inhibitory Control and Attention is a test to measure the inhibitory and attentional facets of Executive Functioning
Time Frame
at baseline and 5 weeks of rTMS
Title
The effects of rTMS on executive function
Description
The Dimensional Change Card Sort is a task designed to assess cognitive flexibility.
Time Frame
at baseline and 5 weeks of rTMS
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria
Fulfilling the Diagnostic and Statistical Manual for Mental Disorders 5th edition (DSM-V) criteria for ASD and confirmed by Gilliam Asperger Disorder Scale (GADS)
The patient exhibiting adequate understanding and cooperation for the procedure
Exclusion criteria
Patients with ASD exhibiting significant anxiety or contact avoidance, precluding them from cooperating with the procedure
Children with a known diagnosis of seizures
Presence of any metallic implants or devices in the head or neck area
Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mitra Assadi, MD
Phone
302-623-3017
Email
mitra.assadi@christianacare.org
Facility Information:
Facility Name
Mitra Assadi
City
Newark
State/Province
Delaware
ZIP/Postal Code
19713
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mitra Assadi, MD
Phone
302-623-3017
Email
mitra.assadikhansari@christianacare.org
12. IPD Sharing Statement
Plan to Share IPD
No
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Enhancement of Behavioral and Cognitive Outcomes in Autism Spectrum Disorder Via Neurostimulation
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