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Clinical Trials/ACTRN12605000374662
ACTRN12605000374662CompletedNot Applicable

Cognitive-behavioral interventions targeting improved adult asthma control and quality of life.

Woolcock Institute of Medical Research and University of Sydney0 sites300 target enrollmentStarted: September 13, 2005Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
300

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility Criteria

Ages
15 Years to 75 Years (—)
Sex
All

Inclusion Criteria

  • Phase one: (Questionnaire to identify people with asthma and anxiety/panic disorder. Diagnosis of asthma and an asthma related medical visit over the previous 12 months. Ability to give informed consent. Ability to read and write English. Phase two: Patients with one or more panic symptoms as identified in phase one. Significant anxiety scores on the HADS as identified in phase one. Phase three: All participants who complete the CBT intervention sessions.

Exclusion Criteria

  • Phase two: Exclude if: any serious mental illness including bipolar disorder or cyclothymia evidence of psychosis or organic brain syndrome, currently involved in any psychotherapy or counseling, women who reprort being pregnant.

Investigators

Sponsor
Woolcock Institute of Medical Research and University of Sydney

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