Respiratory Training in the Treatment of Transdiagnostic Pathological Anxiety

The University of Texas System (UT)

Status: Enrolling

Conditions: Posttraumatic Stress Disorder; Acute Stress Disorder; Illness Anxiety Disorder; Panic Disorder; Trauma; Adjustment Disorder With Anxious Mood; Generalized Anxiety Disorder; Social Anxiety Disorder; Agoraphobia; Anxiety Disorders

Treatments: Behavioral: Psycho-Education; Device: Capnometry-Guided Respiratory Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT05427708

STUDY00002306

Details and patient eligibility

About

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.

Full 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.

Enrollment: 180 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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180 participants in 2 patient groups

Capnometry-Guided Respiratory Intervention (CGRI)

Experimental group

Description:

If assigned to this condition, participants will be expected to complete twice-daily 17-minute tablet-assisted breathing exercises at home for four weeks. They will also receive brief phone check-ins with their study therapist weekly to review progress and troubleshoot any problems they may be experiencing. Last, these participants will have access to a paced-breathing app that provides audio recordings to maintain specified breathing rates for up to 10 minutes.

Treatment:

Device: Capnometry-Guided Respiratory Intervention

Psycho-Education (PsyEd)

Active Comparator group

Description:

If assigned to the psycho-education condition, participants will watch pre-recorded 20-minute video presentations once-weekly for four weeks. They will meet with a study staff member to watch these videos, who will be available to answer any questions. During these sessions, they will be provided information about the nature and causes of anxiety-related disorders and learn tips for coping with anxiety symptoms when they arise. At the end of their sessions with the therapist, they will receive handouts that will help reinforce what they've learned.

Treatment:

Behavioral: Psycho-Education