Improving Social Communication in Individuals With ASD Using AI (NCT05987774) | Clinical Trial Compass
RecruitingNot Applicable
Improving Social Communication in Individuals With ASD Using AI
United States540 participantsStarted 2023-10-15
Plain-language summary
The purpose of this study is to identify whether researched and commonly used face-to-face interventions can be effectively implemented through artificial intelligence (AI) using an application on the phone or computer. The investigators plan to recruit individuals diagnosed with autism spectrum disorder who demonstrate challenges with social communication. Modules focusing on various difficulties experienced by autistic individuals will provide practice and feedback using voice recognition and feedback. If effective, this intervention can be scaled up to provide cost-effective accessible assistance to individuals, particularly those who do not have access to care or prefer to secure services in the comfort of their own homes.
Who can participate
Age range
3 Years – 35 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Primary diagnosis of autism spectrum disorder (ASD)
* Age of adolescents and adults: between 11-35 years
* Age of minimally verbal children: between 3-5 years
* Ability to engage in social conversation using full sentences for a 20-minute period (adolescents and adults)
* Verbal communication difficulties in an individual targeted area (e.g., empathy) as measured on the communication sample
Participants with a co-occuring diagnosis of ADHD, depression, or social anxiety will not be excluded since these are very common in this population and are often related to or a bi-product of difficulties with social communication.
Exclusion Criteria:
* Non-documented or self-diagnosis of ASD
* At or above 60% correct responding on targeted area of social conversation during conversation probe (adolescents and adults)
* No significant language delay (young children)
* No access to phone or computer for intervention sessions
* Inability to carry on a conversation during the conversation probe
* Apparent intellectual impairment that interferes with the ability to carry on a conversation (e.g., responds only in single words or does not respond to conversation, lack of understanding of questions or content during conversation probe)
* Non-English speaking
* Serious medical or psychiatric issues that may interfere with conversation or the ability to complete the program
* Lack of interest in participating.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Social Communication Sample
Timeframe: Approximately 5-9 weeks per participant (4 weeks of intervention + pre and post measures + for adolescents and adults 1-month follow-up.)