Predicting Treatment Response to Exposure Therapy Using a CO2 Habituation Paradigm in Patients With High Levels of Anxiety Sensitivity
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 70
- Locations
- 2
- Primary Endpoint
- Between-session habituation of self-reported anxiety
Study Overview
Brief Summary
Anxiety disorders affect over a quarter of the population, yet very little is known about the variables that predict treatment outcome. The planned study explores whether a patient's response to a physiological test involving inhalation of carbon dioxide predicts their response to exposure therapy.
Detailed Description
Anxiety Sensitivity (AS) refers to an individual's fear of experiencing anxiety-related symptoms (e.g., dyspnea or heart palpitations) and is a core construct underlying the initiation and maintenance of pathological anxiety. Recent evidence suggests that reducing AS may be critical for the prevention and treatment of anxiety across diagnostic categories. Exposure therapy, an important component of cognitive behavioral therapy (CBT), is one of the most effective treatments for reducing AS, and has been shown to improve symptoms across a number of different anxiety disorders. Meta-analyses reveal an approximately 50% treatment response rate, with the remaining half of patients showing either no response or dropping out of treatment early. Unfortunately, there is a paucity of research exploring which variables predict treatment outcome and there are currently no tests for predicting which patients would benefit the most from exposure therapy. In this study, participants will complete two sessions of a carbon dioxide (CO2) habituation paradigm, a safe and noninvasive physiological test that entails repeated exposures to single vital capacity inhalations of 20% CO2. Both CO2 testing sessions will be completed within a 72-hour time period. Patients then complete a 10-week group-based exposure therapy to determine whether an individual's degree of habituation to CO2 predicts treatment outcome.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Basic Science
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 55 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •DSM-V diagnosis of an Anxiety disorder (Generalized Anxiety Disorder, Social Anxiety Disorder, Panic Disorder, Agoraphobia)
- •Anxiety Sensitivity Index (ASI-3) total score > 29
- •Overall Anxiety Severity and Impairment Scale (OASIS) score > 8
- •Between 18-55 years of age
- •Subject must be "treatment-seeking" and willing to enroll in the 10-week group-based Exposure Therapy
Exclusion Criteria
- •Comorbid Bipolar Disorder, Schizophrenia, Anorexia or Bulimia Nervosa, or Obsessive-Compulsive Disorder
- •Current Substance Use Disorder > moderate (within the past 6 months)
- •Currently taking a psychotropic medication
- •Currently receiving psychotherapy/counseling for anxiety
- •Currently being treated as an inpatient
- •Active suicidal ideation with intent or plan
- •History of neurological, cardiovascular or respiratory problems (e.g., asthma, severe brain injury)
Outcomes
Primary Outcomes
Between-session habituation of self-reported anxiety
Time Frame: Across two days of CO2 testing within a 72-hour window
Maximum anxiety rating on a 10-point rating dial (0=no anxiety to 10=most anxiety ever) during day 1 of CO2 testing minus the maximum anxiety rating during day 2 of CO2 testing
Secondary Outcomes
- Between-session habituation of self-reported dyspnea(Across two days of CO2 testing within a 72-hour window)
- Between-session reduction in avoidance behavior(Across two days of CO2 testing within a 72-hour window)