Anxiety Disorders Clinical Trial
Official title:
Testing an Inhibitory Learning Model of Extinction in Exposure-Based Anxiety Treatment for Youth: Feasibility, Acceptability, and Efficacy
| Verified date | December 2020 |
| Source | University of Colorado, Denver |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Recently, basic research conducted in adults has revealed that fear extinction, or the weakening of a learned fear response, may be best explained by principles of "inhibitory learning." New guidelines for the clinical practice of exposure therapy for anxiety disorders have arisen from research on inhibitory learning, but these guidelines have not yet been empirically tested in youth with anxiety disorders. The overall goal of this research is to investigate the acceptability, feasibility, and efficacy of conducting exposure therapy for anxiety disorders in youth according to clinical guidelines developed from basic research on inhibitory learning principles, using a pilot randomized controlled trial design.
| Status | Completed |
| Enrollment | 28 |
| Est. completion date | December 1, 2020 |
| Est. primary completion date | December 1, 2020 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 7 Years to 17 Years |
| Eligibility | Inclusion Criteria: 1. Primary or secondary diagnosis of an anxiety disorder 2. Ability of both child and caregiver to read and understand English 3. Ability of child and at least one caregiver to attend weekly sessions Exclusion Criteria: 1. Diagnosis of autism spectrum disorder, intellectual development disorder, or limited cognitive functioning (i.e., documented Intelligence Quotient [IQ]<80). 2. Diagnosis of a psychotic disorder or bipolar disorder 3. Severe and current suicidal ideation, history of suicide attempt in past six months, or frequent and persistent self-injurious behavior 4. Diagnosis of a substance use disorder or significant, recent substance use 5. Any youth receiving concurrent individual therapy will also be excluded from the study. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Children's Hospital Colorado | Aurora | Colorado |
| Lead Sponsor | Collaborator |
|---|---|
| University of Colorado, Denver |
United States,
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* Note: There are 17 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in Percentage of Exposure Refusals (Feasibility Measure) | Therapists will record the percentage of exposures the patient refused to complete during the session. | Treatment weeks 5, 6, 7, and 8 | |
| Primary | Change in Latency to Initiating Exposure (Feasibility Measure) | Therapist will record the average amount of time the patient delayed before initiating each exposure in session | Treatment weeks 5, 6, 7, 8 | |
| Primary | Early Treatment Termination (Feasibility Measure) | Information will be collected regarding whether the patient terminated treatment early (before session 9) | Measure will be collected following the patient's termination from treatment | |
| Primary | Change in Homework Completion (Feasibility Measure) | Therapist will record the number of exposure sessions for which the patient completed homework | Treatment weeks 6, 7, 8, and 9 | |
| Primary | Client Satisfaction Questionnaire-8 (CSQ-8) | 8-item measure of patient satisfaction with treatment. The measure is rated on a four-point scale, with possible scores ranging from 8-32. | Week 9 (End of Treatment) | |
| Secondary | Change in Distress Tolerance Scale--Child (DTS-C) | A 15-item self-report measure of difficulties managing distress and related emotions. The measure is rated on a 5-point scale, with possible scores ranging from 15 to 65. Higher scores indicate greater ability to tolerate distress. | Treatment Week 1, Week 5, and Week 9 (End of Treatment) | |
| Secondary | Change in Child Avoidance Measure, Self and Parent Report (CAMS/P) | The CAMS/P are 8-item child- and parent-report (respectively) measures of behavioral avoidance. The measure is rated on a 4-point scale, with possible scores ranging from 0 to 24. Higher scores indicate greater behavioral avoidance. | Treatment Week 1, Week 5, and Week 9 (End of Treatment) | |
| Secondary | Change in Avoidance and Fusion Questionnaire--Youth (AFQ-Y) | A 17-item self-report measure of experiential avoidance and cognitive fusion. The measure is rated on a 4-point scale, with possible scores ranging from 0 to 68. Higher scores indicate greater cognitive fusion and experiential avoidance. | Treatment Week 1, Week 5, and Week 9 (End of Treatment) | |
| Secondary | Change in Parent Acceptance and Action Questionnaire (PAAQ) | A 15-item measure of parent experiential avoidance, or parental actions intended to control the form and frequency of their child's emotional experiences. Items are rated on a 7-point scale, with possible scores ranging from 17 to 105. Higher scores indicate less parental experiential avoidance and less effort to control child emotional experiences. | Treatment Week 1, Week 5, and Week 9 (End of Treatment) | |
| Secondary | Change in Screen for Child Anxiety Related Disorders (SCARED), Self and Parent Report | A 41-item child- and parent-report measure assessing symptoms of anxiety in youth ages 7 to 19. Items are rated on a 3-point scale, with scores ranging from 0 to 82. Higher scores indicate greater anxiety symptoms. | Treatment Week 1, Week 5, Week 6, Week 7, Week 8, and Week 9 (End of Treatment) |
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