- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05841680
A Single-Session Intervention for Families on Waitlists for Child Anxiety Treatment (aSSI)
November 12, 2025 updated by: Florida International University
A Single-Session Intervention for Families on Waitlists for Child Anxiety
Lengthy wait times to access treatment for youth anxiety disorders is a critical issue.
To help address this issue, investigators will pursue the following aims in N = 65 families on waitlists for outpatient youth anxiety psychosocial treatment.
Aim 1 Pilot Phase: Develop and pilot a single session intervention (SSI) tailored for families on waitlists for outpatient psychosocial treatment for youth anxiety disorders.
Investigators will pilot the single session intervention (SSI) with N = 5 families and use cognitive response interviewing to obtain data from parents and children, ensuring the content is understandable and accessible.
The SSI will include psychoeducation on the cognitive behavioral conceptualization of anxiety, introduction to self-regulation strategies to manage physiological manifestations of anxiety, and cognitive restructuring of anxiogenic thoughts.
The SSI will also involve parents and present strategies on how parents can support their children in managing anxious feelings and thoughts.
Investigators will refine the SSI based on these data.
Following the Pilot Phase, investigators will enroll an additional N = 60 families and randomize them to either the SSI (n = 30) or waitlist control (n = 30).
Aim 2 Test Phase Acceptability, and Satisfaction: Examine acceptability of the refined SSI, as well as satisfaction with the SSI.
Investigators hypothesize that users will find the module to be acceptable and will report high satisfaction.
Aim 3 Test Phase Anxiety Outcomes: Demonstrate reductions in youth anxiety symptom severity.
Investigators hypothesize that anxiety symptom severity and impairment will be significantly lower among youth who receive the refined SSI relative to youth on waitlist control.
The main risk or discomfort from this research is that participants might feel uncomfortable answering questions about their behavior and feelings.
Another possible risk is breach of confidentiality that could identify a participant as having elevated levels of anxiety.
The benefits of this SSI would include increasing accessibility and scalability of treatment for youth anxiety disorders.
Overall, this study will provide critically needed data to advance resource efficient treatment options for youth anxiety disorders.
Study Overview
Study Type
Interventional
Enrollment (Actual)
59
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Florida
-
Coral Gables, Florida, United States, 33156
- Florida International University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Be between ages 7 and 17 years
- Endorse clinically elevated anxiety symptoms on either parent or youth report, as indicated by a score > 25 on the Screen for Child Anxiety and Related Emotional Disorders-Child or Parent Versions (SCARED-C/P).
Exclusion Criteria:
- Parent report of past diagnosis of Autism Spectrum Disorder, Intellectual Disability, Bipolar Disorder, Tourette's Disorder, Psychotic Disorders, or Substance Use Disorders
- Show high likelihood of hurting themselves or others
- Not having access/connectivity needed for telehealth video conferencing to complete the module.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Waitlist Control
Participants complete pre, post, and follow-up questionnaires.
They have the option to view the SSI module after completing follow-up questionnaires.
|
|
|
Active Comparator: Single Session Intervention Receivers
Participants complete pre then receive the SSI module.
Then they complete post and follow-up questionnaires.
|
Single Session Intervention (SSI) module for youth with anxiety disorders and their parents.
The SSI module will include psychoeducation on the cognitive behavioral conceptualization of anxiety, introduction to self-regulation strategies to manage physiological manifestations of anxiety, and cognitive restructuring of anxiogenic thoughts.
The SSI module will also involve parents and present strategies on how parents can support their children in managing anxious feelings and thoughts.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Screen for Child Anxiety Related Emotional Disorders - Parent Version at Follow up
Time Frame: 4 weeks after first session
|
Follow up parent rating of youth anxiety symptom severity over the past 3 weeks.
The name of the measure is the Screen for Child Anxiety Related Emotional Disorders - Parent Version (SCARED-P).
The SCARED-P is a parent rated measure of the severity of youths' anxiety symptoms.
Total scores on the SCARED-P range from 0 to 82, with higher scores representing more severe anxiety.
|
4 weeks after first session
|
|
Screen for Child Anxiety Related Emotional Disorders - Child Version at Follow-Up
Time Frame: 4 weeks after first session
|
Follow up child rating of youth anxiety symptom severity over the past 3 weeks.
The name of the measure is the Screen for Child Anxiety Related Emotional Disorders - Child Version (SCARED-C).
The SCARED-C is a child rated measure of the severity of youths' anxiety symptoms.
Total scores on the SCARED-C range from 0 to 82, with higher scores representing more severe anxiety.
|
4 weeks after first session
|
|
Screen for Child Anxiety Related Emotional Disorders - Parent Version at Posttreatment
Time Frame: 1 week after first session
|
Posttreatment parent rating of youth anxiety symptom severity over the past week.
The name of the measure is the Screen for Child Anxiety Related Emotional Disorders - Parent Version (SCARED-P).
The SCARED-P is a parent rated measure of the severity of youths' anxiety symptoms.
Total scores on the SCARED-P range from 0 to 82, with higher scores representing more severe anxiety.
|
1 week after first session
|
|
Screen for Child Anxiety Related Emotional Disorders - Child Version at Posttreatment
Time Frame: 1 week after first session
|
Posttreatment child rating of youth anxiety symptom severity over the past week.
The name of the measure is the Screen for Child Anxiety Related Emotional Disorders - Child Version (SCARED-C).
The SCARED-C is a child rated measure of the severity of youths' anxiety symptoms.
Total scores on the SCARED-C range from 0 to 82, with higher scores representing more severe anxiety.
|
1 week after first session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Anxiety Impact Scale - Parent Version at Posttreatment
Time Frame: 1 week after first session
|
Brief parent-report measure of anxiety-related functional impairment over the past week.
The name of the measure is the Child Anxiety Impact Scale-Parent Version (CAIS-P).
The CAIS-P is a parent rated measure of anxiety-related functional impairment.
Total scores on the CAIS-P range from 0 to 81, with higher scores representing more functional impairment.
|
1 week after first session
|
|
Child Anxiety Impact Scale - Child Version at Posttreatment
Time Frame: 1 week after first session
|
Brief youth-report measure of anxiety-related functional impairment over the past week.
The name of the measure is the Child Anxiety Impact Scale-Child/Adolescent Version (CAIS-C).
The CAIS-C is a parent rated measure of anxiety-related functional impairment.
Total scores on the CAIS-C range from 0 to 81, with higher scores representing more functional impairment.
|
1 week after first session
|
|
Child Anxiety Impact Scale - Parent Version at Follow Up
Time Frame: 4 weeks after first session
|
Brief parent-report measure of anxiety-related functional impairment over the past 3 weeks.
The name of the measure is the Child Anxiety Impact Scale-Parent Version (CAIS-P).
The CAIS-P is a parent rated measure of anxiety-related functional impairment.
Total scores on the CAIS-P range from 0 to 81, with higher scores representing more functional impairment.
|
4 weeks after first session
|
|
Child Anxiety Impact Scale - Child Version at Follow Up
Time Frame: 4 weeks after first session
|
Brief youth-report measure of anxiety-related functional impairment over the past 3 weeks.
The name of the measure is the Child Anxiety Impact Scale-Child/Adolescent Version (CAIS-C).
The CAIS-C is a parent rated measure of anxiety-related functional impairment.
Total scores on the CAIS-C range from 0 to 81, with higher scores representing more functional impairment.
|
4 weeks after first session
|
|
Family Accommodation Scale Anxiety - Parent Version at Posttreatment
Time Frame: 1 week after first session
|
Parent-report measure of the frequency with which parents participate in their child's anxiety-related behaviors (e.g., assisting avoidance, providing reassurance) and modification of family routines because of child anxiety over the past week.
The name of the measure is the Family Accommodation Scale Anxiety - Parent Version (FASA-P).
The FASA-P is a measure of parental accommodation.
Total scores on the FASA-C range from 0 to 36, with higher scores representing more parental accommodation.
|
1 week after first session
|
|
Family Accommodation Scale Anxiety - Child Version at Posttreatment
Time Frame: 1 week after first session
|
Youth-report measure of the frequency with which parents participate in their child's anxiety-related behaviors (e.g., assisting avoidance, providing reassurance) and modification of family routines because of child anxiety over the past week.
The name of the measure is the Family Accommodation Scale Anxiety - Child Version (FASA-C).
The FASA-C is a measure of parental accommodation.
Total scores on the FASA-C range from 0 to 36, with higher scores representing more parental accommodation.
|
1 week after first session
|
|
Family Accommodation Scale Anxiety - Parent Version at Follow Up
Time Frame: 4 weeks after first session
|
Parent-report measure of the frequency with which parents participate in their child's anxiety-related behaviors (e.g., assisting avoidance, providing reassurance) and modification of family routines because of child anxiety over the past 3 weeks.
The name of the measure is the Family Accommodation Scale Anxiety - Parent Version (FASA-P).
The FASA-P is a measure of parental accommodation.
Total scores on the FASA-C range from 0 to 36, with higher scores representing more parental accommodation.
|
4 weeks after first session
|
|
Family Accommodation Scale Anxiety - Child Version at Follow Up
Time Frame: 4 weeks after first session
|
Youth-report measure of the frequency with which parents participate in their child's anxiety-related behaviors (e.g., assisting avoidance, providing reassurance) and modification of family routines because of child anxiety over the past 3 weeks.
The name of the measure is the Family Accommodation Scale Anxiety - Child Version (FASA-C).
The FASA-C is a measure of parental accommodation.
Total scores on the FASA-C range from 0 to 36, with higher scores representing more parental accommodation.
|
4 weeks after first session
|
|
Client Satisfaction Questionnaire - Parent Report at Posttreatment
Time Frame: 1 week after first session
|
Parent report measure of consumer satisfaction with services received (e.g., "How would you rate the quality of the services you received?" and "If a friend were in need of similar help, would you recommend our program to him or her?").
The name of the measure is Client Satisfaction Questionnaire (CSQ-8).
Total scores on the CSQ-8 range from 8 to 32, with higher scores representing more satisfaction with services received.
|
1 week after first session
|
|
Client Satisfaction Questionnaire - Youth Report at Posttreatment
Time Frame: 1 week after first session
|
Youth-report measure of consumer satisfaction with services received (e.g., "How would you rate the quality of the services you received?" and "If a friend were in need of similar help, would you recommend our program to him or her?").
The name of the measure is Client Satisfaction Questionnaire (CSQ-8).
Total scores on the CSQ-8 range from 8 to 32, with higher scores representing more satisfaction with services received.
|
1 week after first session
|
|
Program Feedback Scale - Parent Report
Time Frame: 1 week after first session
|
Parent-report measure of perceived acceptability of a single session intervention (e.g.
"I enjoyed the program").
The name of the measure is the Program Feedback Scale (PFS).
Total scores on the PFS range from 0 to 35, with higher scores representing more acceptability.
|
1 week after first session
|
|
Program Feedback Scale - Youth Report
Time Frame: 1 week after first session
|
Youth-report measure of perceived acceptability of a single session intervention (e.g.
"I enjoyed the program").
The name of the measure is the Program Feedback Scale (PFS).
Total scores on the PFS range from 0 to 35, with higher scores representing more acceptability.
|
1 week after first session
|
|
Screen for Child Anxiety Related Emotional Disorders - Child Version at Pre
Time Frame: first session at baseline
|
Child rating of youth anxiety symptom severity over the past month.
The name of the measure is the Screen for Child Anxiety Related Emotional Disorders - Child Version (SCARED-C).
The SCARED-C is a child rated measure of the severity of youths' anxiety symptoms.
Total scores on the SCARED-C range from 0 to 82, with higher scores representing more severe anxiety.
|
first session at baseline
|
|
Screen for Child Anxiety Related Emotional Disorders - Parent Version at Pre
Time Frame: first session at baseline
|
Parent rating of youth anxiety symptom severity over the past month.
The name of the measure is the Screen for Child Anxiety Related Emotional Disorders - Parent Version (SCARED-P).
The SCARED-P is a parent rated measure of the severity of youths' anxiety symptoms.
Total scores on the SCARED-P range from 0 to 82, with higher scores representing more severe anxiety.
|
first session at baseline
|
|
Child Anxiety Impact Scale - Parent Version at Pre
Time Frame: first session at baseline
|
Brief parent-report measure of anxiety-related functional impairment over the past month.
The name of the measure is the Child Anxiety Impact Scale-Parent Version (CAIS-P).
The CAIS-P is a parent rated measure of anxiety-related functional impairment.
Total scores on the CAIS-P range from 0 to 81, with higher scores representing more functional impairment.
|
first session at baseline
|
|
Child Anxiety Impact Scale - Child Version at Pre
Time Frame: first session at baseline
|
Brief youth-report measure of anxiety-related functional impairment over the past month.
The name of the measure is the Child Anxiety Impact Scale-Child/Adolescent Version (CAIS-C).
The CAIS-C is a parent rated measure of anxiety-related functional impairment.
Total scores on the CAIS-C range from 0 to 81, with higher scores representing more functional impairment.
|
first session at baseline
|
|
Family Accommodation Scale Anxiety - Parent Version at Pre
Time Frame: first session at baseline
|
Parent-report measure of the frequency with which parents participate in their child's anxiety-related behaviors (e.g., assisting avoidance, providing reassurance) and modification of family routines because of child anxiety over the past month.
The name of the measure is the Family Accommodation Scale Anxiety - Parent Version (FASA-P).
The FASA-P is a measure of parental accommodation.
Total scores on the FASA-C range from 0 to 36, with higher scores representing more parental accommodation.
|
first session at baseline
|
|
Family Accommodation Scale Anxiety - Child Version at Pre
Time Frame: first session at baseline
|
Youth-report measure of the frequency with which parents participate in their child's anxiety-related behaviors (e.g., assisting avoidance, providing reassurance) and modification of family routines because of child anxiety over the past month.
The name of the measure is the Family Accommodation Scale Anxiety - Child Version (FASA-C).
The FASA-C is a measure of parental accommodation.
Total scores on the FASA-C range from 0 to 36, with higher scores representing more parental accommodation.
|
first session at baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 10, 2023
Primary Completion (Actual)
June 9, 2025
Study Completion (Actual)
October 1, 2025
Study Registration Dates
First Submitted
February 24, 2023
First Submitted That Met QC Criteria
April 24, 2023
First Posted (Actual)
May 3, 2023
Study Record Updates
Last Update Posted (Actual)
November 24, 2025
Last Update Submitted That Met QC Criteria
November 12, 2025
Last Verified
October 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-23-0040
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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