Adapting Anxiety Intervention for Youth With Autism for Rapid Response to COVID-19

Phase

N/A

Condition

Williams Syndrome

Autism

Asperger's Disorder

Treatment

N/A

Clinical Study ID

NCT04666493

0240

Ages 8-13
All Genders

Study Summary

This study will examine if a virtual delivery of a group Cognitive Behavioural Therapy (CBT) program, specifically using "Facing Your Fears" (FYF) curriculum, is helpful in improving anxiety symptoms for children and youth with ASD. This study will adapt the FYF program for virtual delivery using a platform called "Zoom for Healthcare" and examine its effectiveness.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Chronological age between 8 and 13 years (13 yr, 11 mos, 29 days)
Have a clinical diagnosis of Autism Spectrum Disorder (ASD)
Ability to read at a grade 2 level or above (based on parent report)
Verbally fluent at a grade 2 level or above (can speak or respond to questions thatare appropriate for a child in grade 2; based on parent report)
Child with significant anxiety symptoms as determined by the clinical team
To enhance generalizability of our findings, children will be eligible if they presentwith some other co-morbid psychiatric conditions (see exclusion criteria)
If already receiving pharmacological interventions, must meet the following criteria:If receiving concomitant medications for anxiety, must be on a stable dose during themonth prior to screening (6 weeks for fluoxetine).

Exclusion

Exclusion Criteria:

Being currently enrolled in another active behavioral/ educational/ psychologicaltreatment for anxiety
Diagnosis of acute psychosis or conduct disorder, or a primary diagnosis of ObsessiveCompulsive Disorder without another anxiety diagnosis or clinically significant levelof anxiety.

Study Design

December 04, 2020

November 30, 2021

Study Description

The research team will adapt the Facing Your Fears (FYF) program, in consultation with program developers, Canadian experts (psychologists) and Holland Bloorview's Research Family Engagement Committee, to allow for virtual delivery of a traditionally in-person intervention. Adaptations will build on preliminary work already piloted by program developers to meet the current needs (e.g., group work with individual support, video practice for exposures, psychoeducation format).

Participants will complete one screening phone call and one videoconferencing (Zoom for Healthcare) call with the research team, where the delegated research staff will introduce the program and obtain consent for interested and eligible participants. Participants will be asked to provide consent, then proceed to the second part of the screening to ensure that potential participants meet all eligibility criteria. It will be made clear to participants that providing consent and assent at this time will not guarantee study enrollment.

Once eligibility is confirmed, participants will be enrolled in the study and be asked to provide the study team with the participant's ASD diagnostic letter via a secure link (using Sync), complete pre-intervention questionnaires before the start of the program, and post-intervention questionnaires after completing the study intervention.

The program will be abbreviated from 14 weeks to 12 weeks to maximize the number of families served during the study period. Each session will be approximately 60-90 minutes (30-45 minutes with parents and children; 30-45 minutes with parents alone). There will be two check-in calls (approximately 30 mins) with each of the families after weeks 7 and 9 of the program. The group facilitators will use the Zoom for Healthcare platform to deliver the intervention virtually.

Connect with a study center

Holland Bloorview Kids Rehabilitation Hospital
Toronto, Ontario M4G 1R8
Canada
Active - Recruiting

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