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Trial registered on ANZCTR
Registration number
ACTRN12606000177550
Ethics application status
Approved
Date submitted
12/05/2006
Date registered
16/05/2006
Date last updated
16/05/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Preventing the development of panic disorder in vulnerable patients with chronic obstructive pulmonary disease
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Scientific title
Psychological and physiological correlates of panic disorder in patients with chronic obstructive pulmonary disease, and efficacy of prevention of panic anxiety using cognitive behaviour therapy
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Universal Trial Number (UTN)
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Trial acronym
Anxiety in COPD project
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Chronic obstructive pulmonary disease (COPD)
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Condition category
Condition code
Respiratory
1230
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Chronic obstructive pulmonary disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
20 patients with COPD receive a one hour session of cognitive behaviour therapy per week for four weeks - this is the intervention. All continue to receive active treatment as usual for their COPD. All subjects are then assessed every six months over an 18 month follow-up period.
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Intervention code [1]
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Prevention
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Comparator / control treatment
20 control patients with COPD don't receive this intervention.
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Control group
Active
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Outcomes
Primary outcome [1]
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The effectiveness of the brief, standardised CBT intervention in decreasing the likelihood that patients will develop symptoms of panic disorder
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Assessment method [1]
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Timepoint [1]
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An assessment session every six months over 18 month follow-up period.
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Secondary outcome [1]
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To reduce the personal and economic burder associated with the development of panic disorder in COPD patients.
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Assessment method [1]
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Timepoint [1]
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An assessment session every six months over 18 month follow-up period.
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Eligibility
Key inclusion criteria
Diagnosis of COPD, with no age limits on enrolment.
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Minimum age
No limit
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Lack of written fluency in EnglishA co-existing severe disease and/or mental illness.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 1 / Phase 2
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
7/04/2003
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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The Prince of Wales Hospital
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Address [1]
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Country [1]
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Australia
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Funding source category [2]
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University
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Name [2]
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The University of Sydney
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Address [2]
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Country [2]
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Australia
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Primary sponsor type
Individual
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Name
Nicole Livermore (enrolled in part-time PhD degree at University of Sydney
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Address
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr. Louise Sharpe, School of Psychology, University of Sydney, (N. Livermore's primary supervisor)
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Address [1]
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Prince of Wales Hospital
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Ethics committee address [1]
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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29/05/2002
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Ethics approval number [1]
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02/120
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Ethics committee name [2]
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University of Sydney
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Ethics committee address [2]
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
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Approval date [2]
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10/09/2002
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Ethics approval number [2]
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2998
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Summary
Brief summary
40 patients with COPD are randomly allocated to either receive a four session preventative CBT intervention, or not receive this intervention in addition to usual treatment. Subjects are then followed up every six months for 18 months to investigate the efficacy of the intervention in preventing the development/worsening of panic anxiety symptoms.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr. Louise Sharpe
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Address
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School of Psychology
University of Sydney
F - 12 Transient Building
Camperdown NSW 2006
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Country
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Australia
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Phone
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+61 2 93514558
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Fax
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+61 2 93517328
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr. Louise Sharpe
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Address
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School of Psychology
University of Sydney
F - 12 Transient Building
Camperdown NSW 2006
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Country
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Australia
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Phone
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+61 2 93514558
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Fax
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+61 2 93517328
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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