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RUBIES Intervention for Autism (RUBIES Trial)
N/A
Recruiting
Research Sponsored by Seattle Children's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Paraeducators must be employed by the school district and work directly with children with ASD in the classroom at their school
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial tests the RUBIES program, which trains school staff to manage disruptive behaviors in elementary-school children with autism. The goal is to create a more supportive learning environment by teaching effective behavior management techniques. The RUBI program was initially developed for parents of children with autism spectrum disorder (ASD) and challenging behavior in clinic settings.
Who is the study for?
This trial is for elementary-school children with Autism Spectrum Disorder (ASD) who show disruptive behavior. They must be in K-5th grade, spend at least 4 hours a week in general education, have an ASD diagnosis with certain test scores, and exhibit irritability above a set threshold. Their educational plan should be stable, and they need to have a paraeducator willing to participate.
What is being tested?
The study compares the RUBIES intervention—a program delivered by paraeducators—to usual care training for managing disruptive behaviors in kids with ASD. The goal is to see if RUBIES can reduce these behaviors more effectively than standard practices.
What are the potential side effects?
Since this trial involves behavioral interventions rather than medications, traditional side effects are not expected. However, there may be changes in behavior or emotional responses as participants adjust to new strategies used during the intervention.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I work in a school and directly help children with ASD.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Aberrant Behavior Checklist
Secondary study objectives
Knowledge of Behavioral Principles
RUBIES fidelity
Student Behavior Observation
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: RUBIESExperimental Treatment1 Intervention
RUBIES provides paraeducators in training on behavioral strategies based on principles of applied behavior analysis to target student disruptive behaviors in the classroom
Group II: Usual Care TreatmentActive Control1 Intervention
Usual Care Treatment provides paraeducators with foundational psychoeducation on autism spectrum disorders.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RUBIES
2019
N/A
~40
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Behavioral interventions for Autism Spectrum Disorder (ASD), such as Applied Behavior Analysis (ABA), work by using reinforcement strategies to improve social, communication, and learning skills. These methods involve breaking down tasks into smaller steps and using positive reinforcement to encourage desired behaviors.
This approach is essential for ASD patients as it targets core symptoms and helps reduce disruptive behaviors, thereby enhancing their overall quality of life and functional abilities.
Pharmacological and dietary-supplement treatments for autism spectrum disorder: a systematic review and network meta-analysis.What are we targeting when we treat autism spectrum disorder? A systematic review of 406 clinical trials.Commentary: Randomized controlled trials in autism spectrum disorder: state of the field and challenges for the future.
Pharmacological and dietary-supplement treatments for autism spectrum disorder: a systematic review and network meta-analysis.What are we targeting when we treat autism spectrum disorder? A systematic review of 406 clinical trials.Commentary: Randomized controlled trials in autism spectrum disorder: state of the field and challenges for the future.
Find a Location
Who is running the clinical trial?
Seattle Children's HospitalLead Sponsor
310 Previous Clinical Trials
5,230,840 Total Patients Enrolled
7 Trials studying Autism Spectrum Disorder
7,963 Patients Enrolled for Autism Spectrum Disorder
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a student with ASD, meet specific test score criteria, and have a stable school placement.Students with ASD who meet the following criteria will be included in the study: they have a documented ASD diagnosis and a Social Responsiveness Scale-2 total raw score > 70 for males and 65 for females; they are enrolled in a Kindergarten-5th grade general or special education classroom and participate in a general education classroom for a minimum of 4 hours/week; they have a participating paraeducator; they have a teacher-rated Aberrant Behavior Checklist-Irritability (ABC-I) subscale score >15; and they have a stable educational plan and placement.I work with children with ASD in a classroom and am employed by the school district.I work in a school and directly help children with ASD.
Research Study Groups:
This trial has the following groups:- Group 1: Usual Care Treatment
- Group 2: RUBIES
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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