Anxiety Disorders Clinical Trial
Official title:
Targeting Approach Behaviors in Exposures With Self-distancing to Improve Outcomes in Pediatric Anxiety and Obsessive Compulsive Disorders
NCT number | NCT06339463 |
Other study ID # | AAAU7985 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 2024 |
Est. completion date | May 2025 |
Self-Distancing is a cognitive technique that involves shifting perspective away from first person to promote an adaptive, self-reflective stance in emotionally charged situations. This trial aims to help learn how self-distancing may increase approach during exposure and thereby improve treatment response. To find out if self-distancing works by helping children approach fear inducing stimuli, the study will look at behaviors related to approach as well as symptom severity, before, after and during treatment. The study hypothesizes that Self-Distancing will produce greater increases in approach behaviors and greater decreases in anxiety severity than in the Classic Exposure.
Status | Not yet recruiting |
Enrollment | 35 |
Est. completion date | May 2025 |
Est. primary completion date | May 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 7 Years to 17 Years |
Eligibility | Inclusion Criteria: 1. Age 7-17.99 years at time of consent 2. Written informed consent by a parent/legal guardian and assent by child 3. Has a primary clinical diagnosis (diagnosis with the highest CSR) of one of the following Diagnostic and Statistical Manual-5 (DSM-5) Disorders: Separation Anxiety Disorder, Specific Phobia, Social Anxiety Disorder, Panic Disorder, Agoraphobia, Generalized Anxiety Disorder, and/or Obsessive-Compulsive Disorder (OCD) 4. Fluent in English (Participant may be bilingual, but must be able to speak and understand fluent English to participate in study) Exclusion Criteria: 1. Current or past manic/hypomanic episode 2. Current or past psychotic symptoms 3. Autism spectrum disorder diagnosis or elevated symptoms 4. Active alcohol or substance dependence 5. Co-primary clinical diagnosis (CSR = 4) other than Separation Anxiety Disorder, Specific Phobia, Social Anxiety Disorder, Panic Disorder, Agoraphobia, Generalized Anxiety Disorder, and/or Obsessive-Compulsive Disorder (OCD). Other clinical diagnoses are not exclusionary, provided that they are not co-primary or primary (i.e., equal or greater Clinical Severity Rating) 6. Active suicidal ideation or suicidal behavior within the past 3 months prior to baseline assessment 7. Engagement in non-suicidal self-injurious behavior within 6 months prior to baseline 8. Any major medical or neurological problem (e.g., unstable hypertension, seizure disorder, head trauma) 9. Intelligence Quotient < 81 10. Change in psychotropic medication within 1 month of baseline visit 11. Receiving concurrent psychotherapy 12. History of exposure therapy within last 24 months 13. Exposure not appropriate treatment recommendation (e.g., comorbid condition requires different or tailored treatment or higher level of care) |
Country | Name | City | State |
---|---|---|---|
United States | Columbia University Irving Medical Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University |
United States,
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Child Yale-Brown Obsessive-Compulsive Scale (CY-BOCS) | The CY-BOCS is a clinician-rated measure administered to children and caregivers in a semi-structured manner to assess presence and severity of obsessive-compulsive disorder symptoms. The CY-BOCS includes a checklist of obsessions and compulsions, as well as a series of items to assess the severity of obsessions and compulsions. Items are rated 0-5, with higher scores indicating greater severity of symptoms. | Baseline (Week 0), Week 1, Post-Treatment (Week 11) | |
Other | Screen for Child Anxiety Related Disorders (SCARED)- Parent and Child | The SCARED is 41-item measure with parallel forms for youth and caregivers that indexes five domains of anxiety. The SCARED is a robust measure with excellent support for its psychometric properties. Items are rated 0=Not true or hardly ever true to 2=Very true or often true, with higher scores indicating more severe symptoms. | Baseline (Week 0), Mid-Treatment (Week 5), Post-Treatment (Week 11) | |
Other | Obsessive-Compulsive Inventory - Child Version (OCI- CV) | The OCI-CV is an 18-item measure that assesses youth report of obsessive-compulsive symptoms commonly seen in youth. Items are rated 0-4, 0=Not at all and 4=Extremely. | Baseline (Week 0), Mid-Treatment (Week 5), Post-Treatment (Week 11) | |
Other | Toronto Obsessive Compulsive Scale, Parent version (TOCS) | The TOCS is a 21-item measure of OCD symptoms. The parent-report version provides report of obsessive-compulsive symptoms commonly seen in youth. Items are rated on a 7-point Likert scale from -3= far less often, to 3= far more often. | Baseline (Week 0), Mid-Treatment (Week 5), Post-Treatment (Week 11) | |
Other | Clinical Global Impression of Severity (CGI-S) Scale | The CGI-S is a single item severity score clinicians assign about the global severity of anxiety symptoms a patient is experiencing. The CGI-S score range is 1-7, 1=Normal and 7=Among the extremely ill patients. This measure will be completed by independent evaluators at Baseline and Post-treatment, and by the treating clinicians at all therapy session time points. | Baseline, up to Week 12 | |
Other | Clinical Global Impression of Improvement (CGI-I) Scale | The CGI-I is a single item severity score clinicians assign about the global severity of anxiety symptoms a patient is experiencing. The CGI-I score range is 1-7, 1=Very much improved and 7=Very much worse. This measure will be completed by independent evaluators at Baseline and Post-treatment, and by the treating clinicians at all therapy session time points. | Baseline, up to Week 12 | |
Primary | Treatment Engagement and Adherence Ratings (TEARS) | The TEARS is a brief questionnaire assessing youth and therapist reports of youth's adherence to their assigned exposure condition (EXC vs EXSD), and their approach toward the exposure. Adherence and engagement are rated on a Likert scale from 1-7, with higher scores indicating greater engagement and adherence. | Week 3, 4, 5, 6, 7, 8, 9, 10 | |
Secondary | Anxiety Disorders Interview Schedule for DSM-5 (ADIS) Clinical Severity Rating (CSR) | The Anxiety Disorders Interview Schedule for DSM-5 (ADIS) is a structured clinical interview that is adapted for DSM-5 and allows clinicians to ascertain the presence of DSM-5 anxiety disorders or OCD, as well as relevant rule-out diagnoses (e.g., PTSD, bipolar disorder). The ADIS includes clinical severity ratings (CSR) for each diagnosis to allow for easy tracking of the principal and secondary diagnoses, as well as change in severity and remittance status over time. The CSR score range is 0-8, 0= Absence of symptoms/No disturbance in functioning/No disability and 8= Very severe symptoms/Very severe disturbance in functioning/Very severely disabling. The ADIS will be administered to participants and caregivers by a clinician with prior ADIS training and experience. | Pre-treatment (Baseline) and post-treatment assessments (approximately 12 weeks) |
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