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Consultee-centered administrative consultation for Autism
N/A
Waitlist Available
Research Sponsored by Michigan State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 23-26 weeks
Awards & highlights
Study Summary
This triallooks at how consultation can help parents treat autism in their kids in a low-resource setting. It identifies what makes the consultation successful.
Eligible Conditions
- Autism
- Autism Spectrum Disorder
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 23-26 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~23-26 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Case penetration
Child social communication skills
Parent-mediated intervention competence
+3 moreTrial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Treatment (Consultation)Experimental Treatment1 Intervention
Consultation will be conducted in 4-week phases that correspond to the three consultation components. The phases will occur in a randomized order. During a given phase, no components of any other phases will be provided. Feedback phase. Consultees will submit 5-minute clips of session recordings of their Project ImPACT session with their enrolled family for feedback. Oral feedback will be provided by the consultant and peers. Case support phase. The consultant will lead the group in problem-solving common barriers that providers experience with their cases. Skill rehearsal phase. The consultant will lead skill rehearsal practices in which providers role play elements of a Project ImPACT session.
Group II: BaselineActive Control1 Intervention
Following completing the online tutorial, each agency will have a baseline lasting 3-6 weeks (this will be staggered by agency).
Group III: Follow UpActive Control1 Intervention
During the follow-up period, consultation will not occur, and providers will continue implementing Project ImPACT with their cases. Eight weeks post-consultation, providers will submit a recorded Project ImPACT session with their enrolled family. Providers and caregivers will complete a final online questionnaire.
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Who is running the clinical trial?
Michigan State UniversityLead Sponsor
184 Previous Clinical Trials
601,384 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any openings currently available for participation in this experiment?
"The available information on clinicaltrials.gov indicates that, as of the most recent edit date of November 3rd 2022, this medical trial is not currently enrolling patients. Despite this fact, 271 other studies are actively recruiting participants at present."
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