Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 12:00 PM
Ignite Modification Date:
2025-12-24 @ 12:00 PM
NCT ID:
NCT03537261
Eligibility Criteria:
Inclusion Criteria:
* Each subject must be an adult caregiver/parent of a Lurie Center for Autism patient with 'patient' defined as having at minimum one visit/contact per year with any Lurie Center for Autism clinician. The patient (child):
* May be male or female.
* Must be from 5-12 years of age (inclusive).
* Must live at home.
* May have any IQ.
* Must have an ASD diagnosis per the DSM-5 checklist confirmed by expert clinician at enrollment.
* Must have a symptom severity score of 18 or greater on the ABC Irritability subscale confirmed by expert clinician at enrollment.
* The subject may have any primary language but must be comfortable speaking and reading English without translation.
* The subject must be the self-identified primary caregiver of the Lurie Center for Autism patient.
* The subject must be recommended by a Lurie Center for Autism clinician.
* The subject must be able to attend in person the maximum the training session on the specified date/time/location.
* The subject must be willing to complete the assessment measures.
* Only one subject per family may participate.
Exclusion Criteria:
* The subject must not have any self-identified physical limitations or disabilities that prevent use of physical intervention techniques.
* The patient (child) of the subject must not have any compromising neurological disorders (i.e., CP, active seizures).
* The patient should not have the addition of non-drug treatment (including ABA and parent-training) for 4 weeks prior to intervention
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
5 Years
Maximum Age:
12 Years
Study:
NCT03537261
Study Brief:
Protocol Section:
NCT03537261