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Recruiting NCT07624448

Regulating Together for Intellectual Disability and Autism: A Group Behavioral Therapy for for Emotion Dysregulation

No phase Interventional Autism Intellectual Disabilities With Other Behavioral Symptoms Intellectual Disability

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: Regulating Together group therapy.
Who it may be relevant to
Registry conditions: Autism, Intellectual Disabilities With Other Behavioral Symptoms, Intellectual Disability. Basic parameters: 8 years — 12 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

Adapting a Group Intervention for Emotion Dysregulation in Autism and Intellectual Disability

Overview

The goal of this study is to help children with autism and a co-occurring intellectual disability and their families learn practical strategies for managing issues like irritability, aggression, and other challenging behaviors. The main objective of this study is: To adapt current Regulating Together materials to create an outpatient group program for emotion dysregulation in autism and co-occurring intellectual disability (ASD + ID) that will improve psychosocial outcomes for youth with ASD + ID.

Detailed description

Up to ten children with autism and co-occurring Intellectual Disability (ASD + ID) ages 8 to 12 years and their caregivers will be enrolled in the study. This study is being done to develop and test a behavior therapy to help children with ASD + ID calm their emotions. Participants will complete assessments at five time points:

Screening (T1); Week 0: Baseline visit (T2); Week 5: Post Active Treatment (T3); Week 10: 5 week follow-up (T4); and Week 15: 10 week follow-up (T5). Participants will receive 5 weeks of intervention, twice per week, following the T2 visit.

Interventions

  • Behavioral Regulating Together group therapy
    Regulating Together is the original curriculum developed for autistic youth that uses evidence-based therapeutic strategies including relaxation techniques, parent management training, and mindfulness to help regulate emotions. This study will adapt the original Regulating Together curriculum to focus on behavioral interventions to treat emotion dysregulation in Autism with a co-occurring intellectual disability.

Primary outcome measures

  • Emotion Dysregulation Inventory - Reactivity [Time frame: From enrollment to the end of their follow up appointment, about 10 weeks after therapy has completed]
Secondary outcome measures (6)
  • Caregiver and Child Readiness and Satisfaction Surveys [Time frame: From enrollment to end of follow up at 15 weeks]
  • Emotion Regulation Skills Test [Time frame: From enrollment to the end of their follow up appointment, about 10 weeks after therapy has completed]
  • Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety and Depression Scales (Parent-Proxy) [Time frame: From enrollment to the end of their follow up appointment, about 10 weeks after therapy has completed]
  • Clinician Global Impressions - Improvement (CGI-I) [Time frame: From enrollment to the end of their follow up appointment, about 10 weeks after therapy has completed]
  • Parenting Stress Index, 4th Edition, Short Form [Time frame: From enrollment to the end of their follow up appointment, about 10 weeks after therapy has completed]
  • Aberrant Behavior Checklist, 2nd Edition (ABC-2) [Time frame: From enrollment to the end of their follow up appointment, about 10 weeks after therapy has completed]

Eligibility criteria

Child Participant Inclusion Criteria:

  • Males, females, or non-binary youth between 8 and 12 years of age
  • Confirmed diagnosis of Autism Spectrum Disorder (ASD)
  • Confirmed diagnosis of Intellectual Disability
  • Fluent in spoken English.
  • Use of flexible phrase speech or greater
  • Meeting clinically significant emotion dysregulation criteria
  • Willing to participate in twice weekly 90-minute sessions
  • Family is willing to keep prescribed psychiatric medication and outside behavioral interventions stable
  • Parent, guardian, or legally authorized representative (LAR) must provide written permission on behalf of the participant

Child Participant Exclusion Criteria:

  • Initiation of new psychosocial intervention within 30 days prior to first day of treatment
  • Presence of physical aggression in the child directed towards a peer outside the home (i.e., non-siblings) that resulted in injury within 30 days prior to screening. Other significant disruptive, aggressive, self-injurious, or sexually inappropriate behavior felt to be dangerous or overly disruptive to the group sessions will be reviewed by the study team on an individual basis.
  • Presence of comorbid major neuropsychiatric illness warranting other treatment approaches
  • Presence of any major sensory impairment that would limit participating in the material including blindness or uncorrected hearing loss

Caregiver Inclusion Criteria:

  • Age ≥ 18 years
  • Lives and cares for their child with ASD+ID for > 50% of the year
  • Fluent in spoken English.
  • Willing to participate in twice weekly 90-minute sessions, including one virtual session weekly

Caregiver Exclusion Criteria:

-Presence of any major sensory impairment that would limit participating in the material including blindness or uncorrected hearing loss

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

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

United States · 1 center
  • Children's Mercy — Kansas City

Identifiers

NCT: NCT07624448 · STUDY00004069 · KL2TR002367

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗