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Recruiting NCT06593613

Pilot Trial of the RUBI Program for Autistic Adults

No phase Interventional Autism Spectrum Disorder Behavior Parenting

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: RUBI-A, R-ISLEA.
Who it may be relevant to
Registry conditions: Autism Spectrum Disorder, Behavior, Parenting. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Pilot Randomized Trial of the RUBI Program for Families of Autistic Adults

Overview

The goal of this clinical trial is to evaluate if a redesigned version of the RUBI parenting intervention can reduce challenging behaviors and improve adaptive skills in autistic adults with co-occurring challenging behaviors. The main questions it aims to answer are: * Is the redesigned RUBI intervention feasible and acceptable for autistic adults and their families? * Does the redesigned RUBI intervention reduce challenging behaviors and enhance the quality of life for autistic adults? * Researchers will compare the redesigned RUBI intervention to an active control group, Introduction to the Science and Lived Experience of Autism (ISLEA), to see if RUBI is more effective in improving outcomes for autistic adults and their families. Participants will: * Attend sessions where they receive either the RUBI intervention or the ISLEA program. * Engage in activities designed to promote communication, co-regulation, and autonomy in the context of supporting autistic adults. * Complete assessments at the start, throughout, and at the end of the 20-week trial to evaluate outcomes such as challenging behaviors, adaptive skills, and quality of life.

Detailed description

Over the past decade, across three large-scale, NIH-funded trials, the Research Unit in Behavioral Interventions (RUBI) Autism Network developed and systematically tested a low-intensity manualized parenting intervention for autistic children ages 3-14 with challenging behaviors.8-10 RUBI teaches families how to foster home environments that support their autistic child, including teaching parents how to understand their child's behaviors as forms of communication, respond and adapt to their child's unique needs, and personalize strategies for their child's needs and preferences (e.g. utilizing visual supports to align with information processing needs; attuning to the negative impact of unpredictable expectations; accommodating sensory needs). RUBI also may be a promising approach to support families as they provide care and support to their autistic adult dependents.

RUBI has been found to be acceptable to families, reliably delivered by trained therapists, and effective in reducing challenging behaviors and increasing adaptive skills in children.8-10 In response to the shortage of efficacious interventions for autistic adults, RUBI could serve to be systematically redesigned to better support collaboration between family members and their autistic adult dependents, thereby helping autistic adults lead more meaningful and independent lives. To this end, RUBI was recently redesigned utilizing the Discover, Design/Build, Test (DDBT) Framework,11 which leverages user-centered design, participatory action research, and implementation science to ensure that a modified intervention meets the needs of end users (parents, autistic adults, community providers) and is viable across contexts (home, community). Redesign targets included (1) changes in text examples, in-session activities, and language to be more acceptable and relevant to the autistic adult population, (2) content modifications to align focus on supporting communication and dyad co-regulation, (3) improvement in inclusionary and collaborative engagement strategies, and (4) promotion of the autistic adult's engagement, autonomy, and agency during sessions and when implementing strategies.

With the Discover, Design/Build phases successfully completed, a two-year pilot randomized trial will extend our work to the Test phase in order to evaluate the feasibility, acceptability, and efficacy of the newly redesigned RUBI intervention compared to an active control - Introduction to the Science and Lived Experience of Autism (ISLEA). Eighty autistic adults with co-occurring challenging behaviors and their parents will be randomized 1:1 to either RUBI or ISLEA and followed for 20 weeks in order to evaluate key outcomes, including feasibility and acceptability of the redesigned RUBI intervention. This study will also explore the impact of RUBI on autistic adults' challenging behaviors, adaptive skills, and quality of life as well as parent self-efficacy. Successful completion of this proposed pilot study will allow for a future large-scale effectiveness trial of RUBI with autistic adults and their parents.

Interventions

  • Behavioral RUBI-A
    The RUBI-A intervention includes 9 sessions covering Behavioral Principles, Prevention Strategies, Visual Supports, Reinforcement, Co-Regulation, Supporting Communication, Effective Instructions, Teaching Skills, and Generalization and Maintenance. RUBI teaches skills to help build a behavioral "toolbox" for challenging behaviors and adaptive skills. RUBI emphasizes: 1) tailoring the intervention to the specific individual; 2) identifying behavioral function instead of topography to inform behav
  • Behavioral R-ISLEA
    R-ISLEA training focuses on increasing core knowledge and understanding of autism, but it does not provide specific guidance on behavioral strategies for managing challenging behaviors. Developed by autism experts at Drexel University in collaboration with autistic self-advocates, ISLEA is a commercially available psychoeducation program designed for educators, direct support staff, families, caregivers, and autistic individuals. If English is not the language of care for a dyad, subtitles in th

Primary outcome measures

  • Emotion Dysregulation Inventory (EDI) [Time frame: We will use the 24-item Caregiver Reactivity scale for screening, the full 30-item Caregiver form at Baseline, Week 8, Week 16, and Week 20, and the 13-item Self-Report scale at Baseline, Week 8, Week 16, and Week 20.]
  • Open Source Challenging Behavior Scale (OS-CBS) [Time frame: We will administer the OS-CBS to the caregiver at Baseline, Week 8, Week 16, and Week 20.]
  • Aberrant Behavior Checklist (ABC) [Time frame: We will administer the ABC to the caregiver at Baseline and Week 20.]
  • Home Situations Questionnaire - Autism Spectrum Disorder (HSQ-ASD) [Time frame: We will administer the HSQ-ASD to the caregiver at Baseline, Week 8, Week 16, and Week 20.]
  • Top Problems Assessment (TPA) [Time frame: We will administer the TPA to the caregiver and autistic adult at Baseline and weekly through Week 20.]
Secondary outcome measures (10)
  • Adaptive Behavior Assessment System - Third Edition (ABAS-3) [Time frame: We will administer the ABAS-3 to the caregiver at Baseline and Week 20.]
  • World Health Organization QOL Assessment-Brief (WHO-QOL-BRIEF) [Time frame: We will administer the WHO-QOL-BRIEF to the autistic adult at Baseline and Week 20.]
  • RUBI Knowledge Assessment and ISLEA Proximal Knowledge Measure [Time frame: We will administer the knowledge questionnaire to the caregiver and autistic adult at Baseline and Week 16.]
  • Autism-Specific Parenting Self-Efficacy Scale [Time frame: We will administer the self-efficacy scale to the caregiver at Baseline and Week 16.]
  • Zarit-Burden Questionnaire [Time frame: We will administer the Zarit-Burden scale to the caregiver at Baseline and Week 16.]
  • Personal Advocacy Activity Scale (PAAS) [Time frame: We will administer the PAAS to the autistic adult at Baseline and Week 16.]
  • New General Self-Efficacy Scale (NGSE) [Time frame: We will administer the NGSE to the autistic adult at Baseline and Week 16.]
  • Rosenberg Self-Esteem Scale (RSES) [Time frame: We will administer the RSES to the autistic adult at Baseline and Week 16.]
  • Autism and Neurodiversity Attitudes Scale (ANAS) [Time frame: We will administer the ANAS to the autistic adult at Baseline and Week 16.]
  • Neurodiversity Support Scale [Time frame: We will administer the Neurodiversity - Movement Support to the autistic adult at Baseline and Week 16.]

Eligibility criteria

Inclusion criteria

  • Autistic adults will:
  • be age ≥ 18 years;
  • live at home with their parent and be able to attend each session;
  • have a community diagnosis of autism (confirmed through record documentation) and Social Communication Questionnaire (SCQ) total score > 15;
  • have a parent rated 24-item EDI Reactivity Score > 50 percentile, which reflects mild to moderate challenging behaviors (e.g., outbursts; verbal aggression);
  • have receptive language > 18 months as measured on the Mullen Scales of Early Learning (MSEL) Receptive Language subtest or similar measure of receptive language;
  • have a stable educational/vocational plan and be medication free or on stable medication (no changes in prior 6 weeks or planned changes for 16 weeks). Individuals on stable medication will be included as this enhances sample representativeness.
  • Parents/Legally Authorized Representatives will be able to:
  • attend each session.

Exclusion criteria

  • Autistic adults with: (1) serious medical conditions requiring immediate care (e.g., uncontrolled seizures) or (2) serious behavioral challenges where safety to self and/or others is of concern and that warrant more immediate or intensive treatment (e.g., self-injurious behaviors or aggression resulting in tissue damage). This will be evaluated through case panel with study site Principal Investigators.
  • Parents/Legally Authorized Representatives where they are unable to attend weekly virtual or in person sessions over the course of 20 weeks.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 3 centers
  • Els for Autism Foundation — Jupiter
  • A.J. Drexel Autism Institute — Philadelphia
  • Seattle Children's Autism Center — Seattle

Identifiers

NCT: NCT06593613 · SCH STUDY00004782

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗