- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03677089
Extension for Community Healthcare Outcomes Autism Replication Evaluation (ECHO Autism)
ECHO Autism Replication: Step Wedge Randomized Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study involved 10 sites (each referred to as an "ECHO Autism Hub"), each running a 12-session training program using a common curriculum and core lecture, with each site expected to recruit 15 PCPs. Sites were randomized in a stepped-wedge design with 5 clusters (2 sites per cluster) and a staggered start over a 1-year period. Staggering the start allowed for some control for potential temporal trends, as well as allowing the core team to focus on working with each site to ensure smooth startup of the training program at each site.
Outcomes are measured at baseline (Month 0), during the intervention (approximately 3 months after the start of the intervention) and after the end of the intervention (approximately 6 months after the start of the intervention). An additional measurement was made 3 months after the end of the intervention to assess whether deterioration occurs after clinic participation ends.
All participants received the intervention.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Current practice as a primary care provider (PCP)
- Currently providing care for children
- Professional training in: general pediatrics, family medicine, advance practice nursing (i.e. nurse practitioner or physician assistant)
- Active medical license in the state of practice
- Patient population is at least 50% underserved
Exclusion Criteria:
- Trainee status (e.g., medical student, intern, resident, or other pre-professional trainee)
- Subspecialist (e.g., psychiatrists, neurologists, developmental and behavioral pediatricians)
- Practicing within the same practice as another PCP participant (i.e., only one PCP participant from any given practice may be enrolled as a research participant in the study)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: ECHO Cohort
Sites undergo 12 ECHO Autism telehealth clinics.
Clusters of two sites each will initiate intervention with 3 months between the start of each cluster.
|
Twice-monthly 2-hour ECHO Autism Clinics will be provided during a 6-month period.
Each Clinic will include a didactic presentation, 2 to 3 Primary Care Provider-generated case presentations, expert feedback, and group discussion.
Although the ECHO Clinic will include discussion of specific cases, no identifiable personal health information will be shared, individual patients will not be identified, and no direct patient care will be provided.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Longitudinal Pattern of ASD Screening in PCP Charts
Time Frame: Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Clinical Practice/Behavior for ASD screening will be assessed at four time points by review of a subset of charts from each Primary Care Provider's practice.
Four subsets of charts will be reviewed for appropriate ASD screening occurring during well-child visits.
Data will be summarized into the percent of children appropriately screened for ASD by each PCP.
|
Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Longitudinal Pattern of Reported Co-occurring Medical Conditions Correctly Treated in PCP Charts
Time Frame: Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Clinical Practice/Behavior for treating co-occurring medical conditions will be assessed at four time points by review of a subset of charts from each Primary Care Provider's practice.
All visits with an ASD will be reviewed.
Data will be summarized into the percent of co-occurring medical conditions appropriately treated by each PCP.
|
Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Longitudinal Pattern of Scores on Provider ASD Knowledge Assessment
Time Frame: Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
ASD knowledge will be assessed at four time points using a 33-item unpublished test developed specifically for the current study. The test assesses knowledge in the areas of ASD screening/identification, psychiatric co-morbidities, medical co-morbidities, and management of additional ASD-specific needs. This test scores are based on the total number of correct answers, among all 33 questions. Any missing answers are counted as incorrect responses. Scores range from 0-100 with higher scores showing more knowledge of ASD. |
Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Longitudinal Pattern of Scores on Provider ASD Self-Efficacy Assessment
Time Frame: Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Self-Efficacy will be assessed at four time points using a 57-item unpublished questionnaire developed for a previous ECHO Autism pilot study. The questionnaire is comprised of five domains: ASD screening and identification, ASD referral and resources, assessment and treatment of medical comorbidities, assessment and treatment of psychiatric comorbidities, and other items. Primary Care Providers report the degree to which they are confident in their ability to provide effective care in each domain. Items are rated on a 6-point Likert-type scale, where 1 = "no confidence" and 6 = "highly confident/expert". Items are summed for a total score and five sub-scale scores. A subscale is marked as missing if more than 20% of responses are missing and the total score is marked as missing if any subscale is marked as missing or if 6 or more of the 57 questions have missing responses. These scores are then normalized to a percentage. Higher scores indicate greater perceived self-efficacy. |
Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Longitudinal Pattern of the Number of Perceived Barriers to Care
Time Frame: Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Perceived barriers to caring for children with autism in primary care will be assessed by participant response to an unpublished 9-item checklist and an open response "other" category for a total of 10 possible barriers.
A maximum of 10 barriers can be reported and a minimum of 0.
More reported barriers indicate more barriers to care.
|
Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
Participant Satisfaction With ECHO Autism Program
Time Frame: At end of intervention (Month 6)
|
Participant satisfaction will be assessed using an unpublished 12-item survey developed for a previous ECHO Autism pilot study.
The survey includes 10 questions assessing overall satisfaction with participation in the ECHO Autism clinic (rated on a 5-point Likert-type scale), and two questions asking for overall comments and suggestions.
Participant satisfaction is defined as the percentage of participants who answer 2 = "agree" or 1 = "strongly agree" to question 1 ("Participation in ECHO Autism improved my ability to care for children with autism in my practice").
|
At end of intervention (Month 6)
|
PCP ECHO Program Attendance
Time Frame: At end of intervention (Month 6)
|
Percentage of the average number of sessions (out of 12) that the participant attended, of those who have completed the program.
|
At end of intervention (Month 6)
|
Number of Co-morbidities in Children With ASD
Time Frame: Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
|
The summary measure is defined as the mean number of co-morbidities reported among the four co-morbidities of interest for a child with ASD.
Participants can be included in this outcome measure only if they have children with ASD seen in the 60 days prior to the chart review with an identified medical co-morbidity.
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Baseline (Month 0), mid-intervention (Month 3), post-intervention (Month 6), and end of follow-up (Month 9)
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Kristin Sohl, MD, FAAP, University of Missouri Health Care, Thompson Center for Autism
- Principal Investigator: Micah Mazurek, PhD, University of Virginia, Curry School of Education
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2016P000415
- UA3MC11054 (Other Grant/Funding Number: Health Resources and Services Administration)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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