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Respiratory Training in the Treatment of Transdiagnostic Pathological Anxiety

Respiratory Training in the Treatment of Transdiagnostic Pathological Anxiety

Recruiting
18 years and older
All
Phase N/A

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Overview

Purpose of the Research: The primary aim of the proposed study is to conduct a randomized parallel-group 2-arm clinical trial investigating capnometry-guided respiratory intervention (CGRI) for pathological anxiety. CGRI aims to raise end-tidal CO2 levels thereby lowering hyperventilation-induced respiratory alkalosis and its associated fear-eliciting somatic reactions. Psycho-education about anxiety and its effects (PsyEd) will serve as a credible control comparator.

Description

Low end-tidal CO2 (ETCO2), which is an accompanying feature of hyperventilation, has been associated with a variety of anxiety disorders, including panic disorder and social phobia. More recently, researchers have examined the efficacy of capnometry-guided respiratory intervention (CGRI) as a method for increasing ETCO2 and thereby reducing hyperventilation-induced anxiety/panic symptoms. Promising preliminary efficacy studies have shown that CGRI results in decreased panic symptom frequency and severity at a rate comparable to that of cognitive therapy. A recent uncontrolled proof-of-concept study showed that CGRI led to significant reductions in trauma symptoms in a sample of patients meeting DSM-5 criteria for PTSD. However, CGRI has not been adequately evaluated in the treatment of anxiety disorders other than panic disorder with or without agoraphobia.

Eligibility

Inclusion Criteria:

  1. Clinically elevated anxiety as indicated by an eight or higher on the Overall Anxiety Severity and Impairment Scale (OASIS).
  2. Meets DSM-5 criteria for one or more of the following anxiety or trauma-related disorders as their "primary" mental disorder:
    • Generalized Anxiety Disorder
    • Panic Disorder
    • Health Anxiety
    • Agoraphobia
    • Social Anxiety Disorder
    • Posttraumatic Stress Disorder
    • Acute Stress Disorder
    • Adjustment Disorder with primary anxious mood
    • Anxiety disorder not otherwise specified
  3. No current use of psychotropic medications or stable on current medications for at least 6 weeks
  4. Age 18+.
  5. Able to arrange transportation to our laboratory for study appointments.
  6. Fluent in English.

Exclusion Criteria:

  1. No history of medical conditions that would contraindicate participation in fear-provocation or respiratory challenges, including:
    • Cardiovascular or respiratory disorders
    • High blood pressure
    • Epilepsy
    • Strokes
    • Seizures
    • History of fainting
    • Pregnant or lactating
  2. Not currently receiving other psychological treatment for anxiety.
  3. No history of a suicide attempt within the past 6 months.
  4. No history of psychosis within the past 6 months.
  5. No history of moderate to severe alcohol or substance use disorder (with the exception of nicotine) within the past 3 months.
  6. Does not endorse COVID-19 symptoms during the screening phase.

Study details
    Anxiety Disorders
    Trauma
    Generalized Anxiety Disorder
    Panic Disorder
    Agoraphobia
    Illness Anxiety Disorder
    Social Anxiety Disorder
    Posttraumatic Stress Disorder
    Acute Stress Disorder
    Adjustment Disorder With Anxious Mood

NCT05427708

University of Texas at Austin

13 May 2026

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