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Improving the Part C Early Intervention Service Delivery System for Children With ASD

Primary Purpose

Autism Spectrum Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Reciprocal Imitation Training
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autism Spectrum Disorder

Eligibility Criteria

16 Months - 30 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • parents are biological parents or custodial guardians
  • parents are at least 18 years of age
  • parents speak either English or Spanish
  • the child has a diagnosis of ASD or displays social communication impairments
  • The child attends at minimum 1x/week sessions with the enrolled provider

Exclusion Criteria

  • the parent or child has previously received RIT or coaching in another NDBI
  • the child has visual, hearing, or motor conditions that would compromise his/her ability to participate in RIT or assessments

Sites / Locations

  • Rush University Medical CenterRecruiting
  • University of Massachusetts BostonRecruiting
  • Michigan State UniversityRecruiting
  • Carol A SchubertRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

RIT Training Group

Treatment as Usual

Arm Description

Providers in the RIT group (n=80) will receive intensive training (online tutorial, 2-day workshop, and virtual coaching and feedback in the field) in RIT and parent coaching and will be required to achieve fidelity prior to enrolling families from their caseload. They will then be asked to use the intervention with enrolled families for a minimum of 3 months. One intervention session per month for each enrolled family will be videotaped and scored for fidelity. Providers will receive monthly consultation from RIT trainers while these families are in the active treatment phase.

Providers in the TAU group (n=80) will have three sessions videotaped and scored for each enrolled family to assess treatment differentiation. To incentivize agency participation, RIT training will be provided to the TAU group and other providers when data collection is complete.

Outcomes

Primary Outcome Measures

Weighted Frequency of Intentional Communication
The Weighted Frequency of Intentional Communication coding protocol will be used to measure expressive communication during a virtual administration of an adapted version of the Communication Play Protocol (CPP; Adamson et al., 2004). [Hypothesis 1]
Vineland-3
The Communication and Social Domain standard scores from the Vineland-3 will be used to measure child social communication [Hypothesis 1]
Parenting Efficacy Scale (PES)
The PES Total Score will be used to measure parenting efficacy. [Hypothesis 3]
Initiation of Joint Attention
An adapted version of the ESCS coding protocol (Roos et al., 2008) will be used to measure initiation of joint attention within a virtual administration of an adapted version of the Communication Play Protocol (CPP; Adamson et al., 2004). [Hypotheses 2; Putative Mechanism/Mediator]
Unstructured Imitation
An adapted version of the UIA coding protocol (Ingersoll, 2012) will be used to measure spontaneous motor imitation within a virtual administration of an adapted version of the Communication Play Protocol (CPP; Adamson et al., 2004). [Hypotheses 2; Putative Mechanism/Mediator]
Adapted Motor Imitation Scale (MIS)
Elicited motor imitation will be assessed using a virtually-administered version of the Motor Imitation Scale (MIS). [Hypotheses 2; Putative Mechanism/Mediator]
The Parenting Interactions with Children: Checklist of Observations Linked to Outcomes (PICCOLO)
The PICOOLO coding protocol will be used to measure parent responsivity from parent child interaction videos. [Hypotheses 2 & 4; Putative Mechanism/Mediator]
RIT Fidelity Form (RIT-FF)
The RIT-FF will be used to measure parent fidelity of the RIT strategies from parent child interaction videos. [Hypothesis 2; Putative Mechanism/Mediator]

Secondary Outcome Measures

MacArthur Bates Communicative Development Inventory (MCDI)
The total number of words said on the MCDI will be used to measure expressive vocabulary. [Hypothesis 1]
Language Environment Analysis (LENA) Vocal Complexity
Child vocal complexity will be based on recorded language using LENA Software. [Hypothesis 1]
Language Environment Analysis (LENA) Vocal Contingency
Child reciprocal vocal contingency will be based on recorded language using the LENA software. [Hypothesis 1]
Parent Interview for Autism-Clinical Version (PIA-CV)
Social Communication domains from the PIA-CV will be used to measure child social communication. [Hypothesis 1]
Family Life Impairment Scale (FLIS)
The FLIS Total Impairment Score will be used to measure family well-being. [Hypothesis 3]

Full Information

First Posted
October 6, 2021
Last Updated
January 27, 2023
Sponsor
University of Washington
Collaborators
National Institute of Mental Health (NIMH), Michigan State University, Rush University Medical Center, University of Massachusetts, Boston
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1. Study Identification

Unique Protocol Identification Number
NCT05114538
Brief Title
Improving the Part C Early Intervention Service Delivery System for Children With ASD
Official Title
Improving the Part C Early Intervention Service Delivery System for Children With ASD: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 27, 2021 (Actual)
Primary Completion Date
May 31, 2025 (Anticipated)
Study Completion Date
May 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Institute of Mental Health (NIMH), Michigan State University, Rush University Medical Center, University of Massachusetts, Boston

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite strong consensus that early, specialized intervention for children with Autism Spectrum Disorder (ASD) can have a dramatic impact on outcomes, the public health system's capacity to provide such services is severely challenged by the rapid rise in ASD prevalence. The goal of this research project is to increase timely and equitable access to ASD-specialized early intervention during the critical first three years of life by capitalizing on the existing infrastructure of the Part C Early Intervention (EI) system, which is publicly funded and available in all U.S. States. This project will train EI providers to use an evidence-based, inexpensive, parent-mediated intervention that can improve child and family outcomes as well as mitigate the long-term substantial economic costs associated with ASD.
Detailed Description
The long-term goal of this study is to improve services and outcomes for children with early signs of ASD by increasing the capacity to provide appropriately specialized treatment within an existing infrastructure: the Part C Early Intervention (EI) service delivery system. Part C is publicly funded, available throughout the United States, and serves children under age 3 who have developmental delays or disabilities. Currently, the effectiveness of EI services is limited by high practice variation and infrequent use of evidence-based interventions. We are conducting a randomized controlled trial (RCT) to examine the effectiveness of training EI providers to deliver Reciprocal Imitation Training (RIT) to children showing early signs of ASD. RIT is a naturalistic developmental behavioral intervention (NDBI) that is ideally suited for EI settings because it is low intensity, play-based, easy to learn and implement, and can be taught to families for their independent use, thus increasing intervention dosage. This RCT will employ a hybrid type 1 effectiveness/ implementation design and will use a unique mixed methods approach to gather evidence that will be essential for implementing RIT at scale, pending positive trial results. The sample includes 20 EI agencies across 4 U.S. States and comprises a total of 160 EI providers and 440 families of children with early symptoms of ASD, which not only provides a robust sample size, but also affords the opportunity to assess the generalizability of this approach across regions that vary in their implementation of Part C services. EI providers will be randomly assigned to the RIT training group (n=80) or treatment as usual (TAU; n=80). Providers in both groups will identify 2-5 children in their caseload who are 16-30 months old with early symptoms of ASD (n=220 children per group). Intensive, state-of-the art, multimethod assessment technology will be used to measure the impact of the intervention. Child and family assessments will be conducted at baseline, 4 months after enrollment, and 9 months after enrollment. Importantly, this study will examine putative mechanisms through which RIT improves clinically-relevant outcomes. In sum, this study will generate the evidence necessary to implement RIT at scale, thereby increasing the capacity of the existing EI system to deliver effective, evidence-based intervention to the rapidly growing population of children who show early signs of ASD. Hypotheses: Compared to TAU, children assigned to the RIT group will show more growth from baseline (T1) to the 9-month follow-up (T3) on language and social communication. The impact of RIT on children's social communication and language outcomes at T3 will be mediated by gains in: (a) child joint attention; (b) child motor imitation; (c) parent contingent responsivity, and (d) caregiver fidelity of RIT strategies from baseline (T1) to the 4-month follow-up (T2). Compared to TAU, caregivers assigned to the RIT group will show more improvement in parenting efficacy and family quality of life from baseline (T1) to the 9-month follow-up (T3). The impact of RIT on parenting efficacy and family quality of life at T3 will be mediated by gains in parent contingent responsivity from baseline (T1) to the 4-month follow-up (T2).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Enrollement: 440 parent-child dyads; 160 providers (anticipated)
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
440 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RIT Training Group
Arm Type
Experimental
Arm Description
Providers in the RIT group (n=80) will receive intensive training (online tutorial, 2-day workshop, and virtual coaching and feedback in the field) in RIT and parent coaching and will be required to achieve fidelity prior to enrolling families from their caseload. They will then be asked to use the intervention with enrolled families for a minimum of 3 months. One intervention session per month for each enrolled family will be videotaped and scored for fidelity. Providers will receive monthly consultation from RIT trainers while these families are in the active treatment phase.
Arm Title
Treatment as Usual
Arm Type
No Intervention
Arm Description
Providers in the TAU group (n=80) will have three sessions videotaped and scored for each enrolled family to assess treatment differentiation. To incentivize agency participation, RIT training will be provided to the TAU group and other providers when data collection is complete.
Intervention Type
Behavioral
Intervention Name(s)
Reciprocal Imitation Training
Intervention Description
RIT is a relatively straightforward, brief NDBI. It employs four simple strategies to target motor imitation and IJA during play: (1) contingent imitation of the child's verbal and nonverbal behavior, (2) linguistic mapping, (3) direct elicitation of object and gesture imitation following the child's interest, and (4) contingent reinforcement. It has been used at low intensities (e.g., 1-3 hours per week) over short periods of time (e.g., 10-12 weeks) to produce robust changes in pivotal skills. It is easy to learn and can be implemented with fidelity by undergraduate-level therapists with limited backgrounds in ASD, as well as by parents and siblings.
Primary Outcome Measure Information:
Title
Weighted Frequency of Intentional Communication
Description
The Weighted Frequency of Intentional Communication coding protocol will be used to measure expressive communication during a virtual administration of an adapted version of the Communication Play Protocol (CPP; Adamson et al., 2004). [Hypothesis 1]
Time Frame
Change from baseline to 9 months
Title
Vineland-3
Description
The Communication and Social Domain standard scores from the Vineland-3 will be used to measure child social communication [Hypothesis 1]
Time Frame
Change from baseline to 9 months
Title
Parenting Efficacy Scale (PES)
Description
The PES Total Score will be used to measure parenting efficacy. [Hypothesis 3]
Time Frame
Change from baseline to 9 months
Title
Initiation of Joint Attention
Description
An adapted version of the ESCS coding protocol (Roos et al., 2008) will be used to measure initiation of joint attention within a virtual administration of an adapted version of the Communication Play Protocol (CPP; Adamson et al., 2004). [Hypotheses 2; Putative Mechanism/Mediator]
Time Frame
Change from baseline to 4 months
Title
Unstructured Imitation
Description
An adapted version of the UIA coding protocol (Ingersoll, 2012) will be used to measure spontaneous motor imitation within a virtual administration of an adapted version of the Communication Play Protocol (CPP; Adamson et al., 2004). [Hypotheses 2; Putative Mechanism/Mediator]
Time Frame
Change from baseline to 4 months
Title
Adapted Motor Imitation Scale (MIS)
Description
Elicited motor imitation will be assessed using a virtually-administered version of the Motor Imitation Scale (MIS). [Hypotheses 2; Putative Mechanism/Mediator]
Time Frame
Change from baseline to 4 months
Title
The Parenting Interactions with Children: Checklist of Observations Linked to Outcomes (PICCOLO)
Description
The PICOOLO coding protocol will be used to measure parent responsivity from parent child interaction videos. [Hypotheses 2 & 4; Putative Mechanism/Mediator]
Time Frame
Change from baseline to 4 months
Title
RIT Fidelity Form (RIT-FF)
Description
The RIT-FF will be used to measure parent fidelity of the RIT strategies from parent child interaction videos. [Hypothesis 2; Putative Mechanism/Mediator]
Time Frame
Change from baseline to 4 months
Secondary Outcome Measure Information:
Title
MacArthur Bates Communicative Development Inventory (MCDI)
Description
The total number of words said on the MCDI will be used to measure expressive vocabulary. [Hypothesis 1]
Time Frame
Change from baseline to 9 months
Title
Language Environment Analysis (LENA) Vocal Complexity
Description
Child vocal complexity will be based on recorded language using LENA Software. [Hypothesis 1]
Time Frame
Change from baseline to 9 months
Title
Language Environment Analysis (LENA) Vocal Contingency
Description
Child reciprocal vocal contingency will be based on recorded language using the LENA software. [Hypothesis 1]
Time Frame
Change from baseline to 9 months
Title
Parent Interview for Autism-Clinical Version (PIA-CV)
Description
Social Communication domains from the PIA-CV will be used to measure child social communication. [Hypothesis 1]
Time Frame
Change from baseline to 9 months
Title
Family Life Impairment Scale (FLIS)
Description
The FLIS Total Impairment Score will be used to measure family well-being. [Hypothesis 3]
Time Frame
Change from baseline to 9 months
Other Pre-specified Outcome Measures:
Title
Parenting Stress Index-Short Form
Description
Parenting stress will be measured using the Parenting Stress Index-Short Form (PSI-SF) [Moderator]
Time Frame
Baseline
Title
Developmental Play Assessment (DPA
Description
Total number of differentiated acts on toys will be assessed using a virtually-administered version of the Developmental Play Assessment (DPA) [Moderator]
Time Frame
Baseline
Title
Vineland-3
Description
The Adaptive Behavior Composite score will be used to measure child developmental level [Moderator]
Time Frame
Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Months
Maximum Age & Unit of Time
30 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: parents are biological parents or custodial guardians parents are at least 18 years of age parents speak either English or Spanish the child has a diagnosis of ASD or displays social communication impairments The child attends at minimum 1x/week sessions with the enrolled provider Exclusion Criteria the parent or child has previously received RIT or coaching in another NDBI the child has visual, hearing, or motor conditions that would compromise his/her ability to participate in RIT or assessments
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carol A Schubert, MPH
Phone
206-543-2823
Email
schubca@uw.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Wendy K Stone, PhD
Phone
206-685-2821
Email
stonew@uw.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wendy L Stone, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rush University Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anna Hirshman, BA
Email
Anna_Hirshman@rush.edu
First Name & Middle Initial & Last Name & Degree
Allison Wainer, PhD
Facility Name
University of Massachusetts Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02125
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alice Carter, PhD
Email
AliceS.Carter@umb.edu
First Name & Middle Initial & Last Name & Degree
Alice Carter, PhD
Facility Name
Michigan State University
City
East Lansing
State/Province
Michigan
ZIP/Postal Code
48824
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julia Nauman, BS
Email
naumanj@msu.edu
First Name & Middle Initial & Last Name & Degree
Brooke Ingersoll, PhD
Facility Name
Carol A Schubert
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carol A Schubert, MPH
Phone
206-543-2823
Email
schubca@uw.edu
First Name & Middle Initial & Last Name & Degree
Wendy Stone, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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Improving the Part C Early Intervention Service Delivery System for Children With ASD

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