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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05419895
Other study ID # STUDY00003763
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 16, 2022
Est. completion date June 2025

Study information

Verified date March 2024
Source Emory University
Contact Allison Schwartz, PhD
Phone 404.727.8350
Email allison.schwartz@emory.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Babies Can't Wait (BCW) in Georgia will be referring families with children seeking an autism spectrum disorder (autism) diagnosis at the Emory Autism Center's (EAC) Child Screening and Assessment Clinic.The objective of this study is to develop, pilot, and evaluate a diagnostic protocol for children identified at high risk for autism in the BCW early intervention program screening (part of a public health service). This program evaluation will be using pre- and post-data and data collected through the process to evaluate the effectiveness of the EDRM pilot.


Description:

The objective of this study is to develop, pilot, and evaluate a diagnostic protocol to assess high-risk toddlers for autism spectrum disorder (ASD) diagnosis of families enrolled in the Georgia Babies Can't Wait (BCW) early intervention program. The Early Diagnostic Response Model (EDRM) project will be addressing children who are identified at high risk for ASD according to the BCW screening protocol, which is the M-CHAT-R/F. Community psychologist will be taught the protocol and receive referrals to build capacity and better address the need across the state. Currently, many children who are screening high-risk for ASD in BCW districts are unable to access follow-up evaluations due to limited community resources and long wait times. It is hypothesized that the EDRM will be successful in increasing the number of BCW families that access an ASD evaluation using telehealth tools and testing protocols and that the families and clinicians involved will be satisfied with the streamlined process. The clinicians' conclusions from the EDRM assessment will be based on the Diagnostic and Statistical Manual, 5th edition (DSM-5; American Psychiatric Association [APA], 2013) and are hypothesized to be able to provide high-risk children and their families with the same access to services as an in-person assessment. A secondary objective is to investigate how many high-risk referral assessments can be completed entirely via streamlined telehealth protocol and how many required additional information to be collected to make a final DSM-5 conclusion. A tertiary objective is to investigate the improvement of the EDRM as an early identification model to assess for ASD by comparing the numbers of families screened high risk for ASD and referred for an evaluation prior to the study to the number of families who received ASD evaluation by the end of the study through the pilot versus other means. These numbers will be analyzed globally as well as by specific BCW district and other child factors.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date June 2025
Est. primary completion date June 2025
Accepts healthy volunteers No
Gender All
Age group 16 Months to 36 Months
Eligibility Inclusion Criteria: - All families of children between the ages of 16-30 months of age who scored =8 on the MCHAT-R and whose BCW provider refers the child to our clinic by 33 months of age will be a possible participant. Evaluations will be done by 36 months of age. - Referring BCW provider must be one of the three targeted BCW districts participating in this pilot study. - Parent/Guardian needs to have basic English proficiency - Parent/Guardian needs to have internet access - Child must have exposure to English either at home or in out-of-home care (e.g., childcare setting). - Documentation of M-CHAT-R High-Risk failed score (= 8) must be documented in referral. Exclusion Criteria: - Families making self-referrals to the EAC or referrals outside of the targeted BCW districts will be excluded from recruitment for this study. - Children above the age of 33 months at the time of the referral will be excluded as the current EDRM protocol has not been developed in this phase of piloting for individuals over this age. - Non-English speakers will be excluded from participation due to the current protocol not being applicable to their needs as well as a high correlation between verbal language abilities and social communication and social interaction (SCI) abilities as part of the DSM-5-TR autism criteria.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Early Diagnostic Response Model (EDRM)
Use of telehealth capabilities to implement measures and capture and code information related to an autism diagnosis. This program evaluation will be using pre- and post-data and data collected through the process to evaluate the effectiveness of the EDRM pilot.

Locations

Country Name City State
United States Emory Autism Center Atlanta Georgia

Sponsors (2)

Lead Sponsor Collaborator
Emory University Georgia Department of Public Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants referred to the Early Diagnostic Response Model (EDRM) Monthly numbers of high-risk referrals to the EDRM pilot project and total number of referrals made to the EDRM at the end of the study Until the end of the study (approximately one year)
Primary Number of participants consented in the Early Diagnostic Response Model (EDRM) study Monthly number of families referred who consent to EDRM participation Monthly until until the end of the study (approximately one year)
Primary Response rate in the Early Diagnostic Response Model (EDRM) study Response rate will be calculated at project end using the formula [# of families who consented / # of families referred to project] x 100 = response rate) Until end of the study (approximately one year)
Primary Number of participants that completed the Early Diagnostic Response Model (EDRM) study Quarterly numbers of participants that completed the EDRM assessment protocol and total number of participants who completed EDRM assessment protocol at study conclusion Every 3 months (Quarterly) until end of study (approximately one year)
Primary Time from referral to completion of the program Individual calculation of time from BCW referral to final summary report sent to family using the formula:
Date of Final Report sent to family - Date of referral from BCW =Time in EDRM pilot
Up to 12 weeks post-intervention
Secondary Number of high-risk referral assessments that completed entirely via streamlined telehealth protocol Number of high-risk referral assessments that completed entirely via streamlined telehealth protocol, analyzed globally. Monthly, Quarterly, and Total numbers of participants who completed EDRM pilot assessment. Every 3 months (Quarterly) until end of study (approximately one year), Up to 12 weeks post-intervention
Secondary Number of of high-risk referral by BCW district Number of high-risk referral assessments by specific BCW district. Monthly, Quarterly, and Total numbers of participants who completed EDRM pilot assessment. Every 3 months (Quarterly) until end of study (approximately one year), Up to 12 weeks post-intervention
Secondary Number of of high-risk referral by child factors Number of high-risk referral assessments by child factors. Monthly, Quarterly, and Total numbers of participants who completed EDRM pilot assessment. Every 3 months (Quarterly) until end of study (approximately one year), Up to 12 weeks post-intervention
Secondary Number of of high-risk referral by clinician setting Number of high-risk referral assessments by clinician setting. Monthly, Quarterly, and Total numbers of participants who completed EDRM pilot assessment. Every 3 months (Quarterly) until end of study (approximately one year), Up to 12 weeks post-intervention
Secondary Number of participants with additional information collected to make a final DSM-5 conclusion Number of participants with additional information collected to make a final DSM-5 conclusion Every 3 months (Quarterly) until end of study (approximately one year), Up to 12 weeks post-intervention
Secondary Parent satisfaction of EDRM assessment survey Administered at the end of individual EDRM assessment. Satisfaction surveys will use a Likert-scale of 1-5 with 1 being strongly disagree and 5 being strongly agree as well as 0 being not applicable/unknown. Higher scores indicate more satisfaction with specific aspect of EDRM project.
Total score: 0 to 110.
At completion of EDRM assessment (4 weeks post-intervention)
Secondary BCW provider(s) Service Coordinator satisfaction with EDRM assessment survey Administered at end of individual EDRM assessment. Satisfaction surveys will use a Likert-scale of 1-5 with 1 being strongly disagree and 5 being strongly agree as well as 0 being not applicable/unknown. Higher scores indicate more satisfaction with specific aspect of EDRM project.
Total score: 0 to 110.
At completion of EDRM assessment (4 weeks post-intervention)
Secondary Parent satisfaction with access to treatment survey Administered 3-months after completion of EDRM assessment. Satisfaction surveys will use a Likert-scale of 1-5 with 1 being strongly disagree and 5 being strongly agree as well as 0 being not applicable/unknown. Higher scores indicate more satisfaction with specific aspect of EDRM project.
Total score: 0 to 15.
3 months after completion of EDRM assessment
Secondary BCW provider(s) Early Intervention Coordinator satisfaction with EDRM pilot survey Completed every 3 months (Quarterly). Satisfaction surveys will use a Likert-scale of 1-5 with 1 being strongly disagree and 5 being strongly agree as well as 0 being not applicable/unknown. Higher scores indicate more satisfaction with specific aspect of EDRM project.
Total score: 0 to 55
Every 3 months (Quarterly) until end of study (approximately one year), Up to 12 weeks postintervention
Secondary Number of families screened high risk for ASD and referred for an evaluation Number of families screened high risk for ASD and referred for an evaluation Through study completion, an average of 1 year
Secondary Number of families who received ASD evaluation by the end of the study through the pilot versus other means Number of families who received ASD evaluation by the end of the study through the pilot versus other means Through study completion, an average of 1 year
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