CLASSEducator-Delivered RUBIES Intervention and HELM Implementation Strategy for Autistic Children's Externalizing Behaviors in Schools
This study aims to implement the educator-delivered RUBIES intervention and HELM strategy to manage externalizing behaviors in autistic children within a school setting.
RUBIES
+ HELM
+ Educator Psychoeducation
Autism Spectrum Disorder+2
+ Autistic Disorder
+ Mental Disorders
Treatment Study
Summary
Study start date: February 1, 2026
Actual date on which the first participant was enrolled.Schools cater to many children with autism, but face challenges in providing proven practices to manage externalizing behaviors. These challenges include limited availability of effective methods and inconsistent use of these methods over time. This project aims to bridge these gaps by testing two approaches. First, it examines an efficient, teacher-led intervention called RUBIES, designed to reduce externalizing behaviors in children with autism. Second, it evaluates an organizational strategy, HELM, which is tailored to improve the long-term use of proven practices in public schools. The study also explores how these methods work to achieve their respective goals. This research aligns with high-priority areas identified by health authorities, aiming to improve the application of effective interventions in community settings and enhance the adoption and continuous improvement of mental health services. If successful, this study could significantly benefit children with autism in schools across the USA, by providing an effective solution for a common problem and ensuring its sustained, faithful use.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.373 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 5 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
Active ComparatorStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location