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Neurostimulation
Neurostimulation for Autism Spectrum Disorder
N/A
Waitlist Available
Research Sponsored by Christiana Care Health Services
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Must not have
Children with a known diagnosis of seizures
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at baseline and 5 weeks of rtms
Awards & highlights
Summary
This trial will test whether transcranial direct current stimulation (tDCS) can help people with ASD by improving social cognition and communication skills.
Who is the study for?
This trial is for individuals who meet the criteria for Autism Spectrum Disorder (ASD) as per the DSM-V and confirmed by GADS, with an ability to understand and cooperate during procedures. It excludes those with severe anxiety or contact avoidance, a history of seizures, metallic implants in head/neck, or pregnant women.Check my eligibility
What is being tested?
The study explores Trans Cranial Magnetic Stimulation (TMS) as a neurostimulation method to improve social interaction and cognitive functions in people with ASD. The aim is to find an effective treatment beyond current medications that only address some behavioral issues.See study design
What are the potential side effects?
While not explicitly stated here, TMS can sometimes cause discomfort at the stimulation site, headache, lightheadedness, or tingling sensations. Rarely it might induce seizures or affect hearing if proper ear protection isn't used.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My child has been diagnosed with seizures.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at baseline and 5 weeks of rtms
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at baseline and 5 weeks of rtms
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
The effects of rTMS on reciprocal rigid patterns of behavior
The effects of rTMS on reciprocal social cognition
Secondary outcome measures
The effect of rTMS on verbal fluency
The effects of rTMS on executive function
Trial Design
2Treatment groups
Active Control
Group I: right IPL stimulationActive Control1 Intervention
half of the subjects will receive TMS on the right inferior parietal lobule.
Group II: left IPL stimulationActive Control1 Intervention
half of the subjects will receive TMS on the left inferior parietal lobule.
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Who is running the clinical trial?
Christiana Care Health ServicesLead Sponsor
116 Previous Clinical Trials
107,497 Total Patients Enrolled
Dupont Applied BiosciencesIndustry Sponsor
11 Previous Clinical Trials
2,854 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My child has been diagnosed with seizures.I understand and am willing to follow the study procedures.
Research Study Groups:
This trial has the following groups:- Group 1: right IPL stimulation
- Group 2: left IPL stimulation
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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