Promoting Positive Outcomes for Individuals With ASD: Linking Early Detection, Treatment, and Long-term Outcomes

Sponsor
Drexel University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT03333629
Collaborator
University of California, Davis (Other), University of Connecticut (Other)
3,450
3
2
66
1150
17.4

Study Details

Study Description

Brief Summary

Autism spectrum disorder (ASD) is defined by impaired social engagement and social communication, and repetitive, restricted, or stereotyped behaviors and interests. The average age of diagnosis in the US is after the fourth birthday. However, children who start ASD-specific early intervention have better outcomes than children start later. The current study will address a gap identified by the US Prevention Services Task Force, namely that children detected through screening respond positively to early intervention. This study will directly relate early detection strategies to early intervention, and measure the impact of age of intervention onset on outcomes when children are entering kindergarten. Local pediatric providers will be randomized to provide either usual care, or to an experimental condition in which autism early detection strategies are enhanced through the addition of specific procedures. Across all sites, 8,000 children will be recruited through their participating pediatric practice. Qualifying children will receive up to one year of early intensive behavioral intervention, after getting an ASD diagnosis. Primary outcome measures will include children's cognitive functioning and ASD symptom severity, which will be measured at multiple time points. The investigators predict that this study will inform early detection strategies which will result in improving children's social and cognitive functioning, mitigating lifespan disability, reducing societal costs, and improving personal well-being and productivity of individuals with ASD.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Enhanced early detection
Phase 4

Detailed Description

Autism spectrum disorder (ASD) is a serious neurodevelopmental disorder defined by impaired social engagement and social communication, in addition to the presence of repetitive, restricted, or stereotyped behaviors and interests. Although many cases of ASD can be detected when children are less than two years old, the average age of diagnosis in the US is still after the fourth birthday. However, evidence demonstrates that children who start ASD-specific early intervention have better outcomes than children who do not start treatment until later ages. In 2006 and 2007, American Academy of Pediatrics recommended three early detection approaches to improve identification of children at risk for ASD: ongoing developmental surveillance at every well-child check-up, routine broad developmental screening at three infant/toddler ages, and ASD-specific screening at two toddler ages. When these early detection strategies are used with all children attending well-child check-ups, the age of ASD detection is lower, and children who are diagnosed have the opportunity to start ASD-specific early intervention at younger ages than if they had not been detected. Yet in 2016, the US Preventive Services Task Force (USPSTF) indicated that current evidence is insufficient to recommend universal ASD screening, given the lack of experimental studies demonstrating positive outcomes for treated children that are detected through screening. The current study will address this gap. This study will directly relate early detection strategies to early intervention, and measure the impact of age of intervention onset on outcomes when children are entering kindergarten. The study will be conducted by investigators from three sites: Drexel University; the University of California, Davis; and the University of Connecticut. Local pediatric providers will be enrolled in the study, and their practices will be randomized to provide either usual care, or to an experimental condition in which autism early detection strategies are enhanced through the addition of specific procedures. Children attending well-child visits at participating practices will then be enrolled. Across all sites, 8,000 children will be recruited through their participating pediatric practice. As part of the study, qualifying children will receive up to one year of early intensive behavioral intervention, using an evidence-based manualized treatment. Primary outcome measures will include children's cognitive functioning and ASD symptom severity, which will be measured at multiple time points. Exploratory outcomes will include children's adaptive functioning, kindergarten readiness, and social reciprocity, as measured by experimental eye tracking and parent-child interaction ratings. This study also will examine the impact of the screening intervention on physician attitudes and on parent empowerment and stress. Finally, investigators will examine potential moderators of outcomes, to determine whether initial symptom severity, cognitive ability, or socioeconomic status affects children's long-term outcomes. The investigators predict that this study will inform early detection strategies which will result in improving children's social and cognitive functioning, mitigating lifespan disability, reducing societal costs, and improving personal well-being and productivity of individuals with ASD.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
3450 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Screening
Official Title:
Connecting the Dots: An RCT Integrating Standardized ASD Screening, High-Quality Treatment, and Long-Term Outcomes
Actual Study Start Date :
Nov 29, 2017
Anticipated Primary Completion Date :
May 31, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Enhanced early detection

Providers will receive training to administer enhanced early detection strategies.

Behavioral: Enhanced early detection
standardized screening

No Intervention: Usual care

Providers will not change their early detection strategies, but will be monitored.

Outcome Measures

Primary Outcome Measures

  1. Change in ASD Symptom Severity [Change from pre-treatment to immediately post-treatment; 10 minutes]

    ASD symptom severity will be measured with the Brief Observation of Social Communication Change (BOSCC)

  2. Change in Cognitive Functioning [Change from pre-treatment to immediately post-treatment; 60 minutes]

    Cognitive functioning will be measured by the Mullen Scales of Early Learning (MSEL).

Secondary Outcome Measures

  1. Adaptive Functioning [Immediately post-treatment, 48 m, 60 m; 45 minutes]

    Vineland Adaptive Behavior Scales-3

  2. ASD Symptoms - secondary measure1 [48 m, 60 m; 45 minutes]

    Autism Diagnostic Observation Schedule, Second Edition (ADOS-2)

  3. Kindergarten Readiness [60 m; 45 minutes]

    Developmental Indicators for the Assessment of Learning-4

  4. Social Engagement [Immediately post-treatment, 48 m, 60 m; 15 minutes]

    Eye tracking paradigms will assess aspects of social engagement (i.e., social orienting, motivation, and cognition)

  5. Long-term change in Cognitive Functioning [48 m, 60 m; 60 minutes]

    Cognitive functioning will be measured by the Mullen Scales of Early Learning (MSEL)

  6. Parent-Child Social Engagement [Immediately post-treatment, 48 m, 60 m; 15 minutes]

    Parent-child social engagement will be measured with the Joint Engagement Rating Inventory, which is applied to video recordings of the Communication Play Protocol.

  7. ASD symptoms - secondary measure2 [Immediately post-treatment, 48 m, 60 m; 20 minutes]

    PDD Behavior Inventory

  8. ASD symptoms - secondary measure3 [48 m, 60 m; 10 minutes]

    BOSCC

  9. Long-term change in Cognitive Functioning (alternative) [48 m, 60 m; 60 minutes]

    and for children who reach ceiling on the MSEL, we will use the Differential Differential Abilities Scales-II (DAS-II) will be used for children too advanced for Outcome 7

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Months to 58 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • child attended 18 m visiting at participating pediatric practice

  • legal guardian is fluent in English or Spanish

Exclusion Criteria:
  • child has severe sensory or motor deficit that precludes completing standardized evaluation

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of California, Davis Sacramento California United States 95817
2 University of Connecticut Storrs Connecticut United States 06269
3 Drexel University Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • Drexel University
  • University of California, Davis
  • University of Connecticut

Investigators

  • Principal Investigator: Diana Robins, PhD, Drexel University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Diana Robins, Professor, Drexel University
ClinicalTrials.gov Identifier:
NCT03333629
Other Study ID Numbers:
  • R01MH115715
First Posted:
Nov 7, 2017
Last Update Posted:
Sep 24, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Diana Robins, Professor, Drexel University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 24, 2021