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Trial registered on ANZCTR
Registration number
ACTRN12612000750886
Ethics application status
Approved
Date submitted
11/07/2012
Date registered
13/07/2012
Date last updated
13/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
The development of a quality of life instrument specific to autoimmune bullous disease
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Scientific title
The development of a quality of life instrument specific to autoimmune bullous disease: the Autoimmune Bullous Disease Quality of Life instrument (ABQOL)
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Secondary ID [1]
280800
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Quality of life in Autoimmune bullous disease
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Condition category
Condition code
Skin
287185
287185
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0
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Dermatological conditions
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Public Health
287238
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0
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Other public health
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Patients with clinically and histologically diagnosed autoimmune bullous disease will participate in the development of a disease specific quality of life instrument. They will express the ways in which their blistering diseases affects their quality of life. Based on these responses, a pilot questionnaire will be developed. Patients will then be asked to complete the pilot questionnaire once. Statistical analyses will be completed on the responses to determine whether the questionnaire is a statistically sound.
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Intervention code [1]
285231
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Not applicable
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Comparator / control treatment
Nil
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The development of a quality of life instrument specific to autoimmune bullous disease. Once this instrument has been developed and if it is found to be statistically sound, it will be used by other researchers when evaluating quality of life in patients with blistering diseases.
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Assessment method [1]
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Timepoint [1]
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Patient recruitment will cease once approximately 70 patients have been recruited and have completed the pilot questionnaire. This will mark the end of the patient recruitment process and occur at the end of the trial period. Once this target has been reached, statistical review of the results will be completed
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Secondary outcome [1]
298256
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N/A
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Assessment method [1]
298256
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Timepoint [1]
298256
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N/A
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Eligibility
Key inclusion criteria
Clinically and histologically diagnosed autoimmune bullous disease
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Minimum age
18
Years
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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
Limited fluency in English
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Study design
Purpose
Psychosocial
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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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
5/05/2007
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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
70
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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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Self funded/Unfunded
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Name [1]
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Dedee Murrell
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Address [1]
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Department of Dermatology, St George Hospital, Gray Street, Kogarah, NSW, 2217
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Country [1]
285597
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Australia
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Primary sponsor type
Charities/Societies/Foundations
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Name
Australasian Blistering Diseases Foundation
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Address
Department of Dermatology, St George Hospital, Gray Street, Kogarah, NSW, 2217
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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University of New South Wales Independent Learning Program
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Address [1]
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Faculty of Medicine
The University of New South Wales
Sydney NSW 2052
Australia
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Country [1]
284429
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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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South Eastern Sydney and Illawarra Area Health Service Human Research Ethics Committee
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Ethics committee address [1]
287598
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
287598
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Approval date [1]
287598
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Ethics approval number [1]
287598
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Summary
Brief summary
The purpose of this project is to develop a quality of life instrument specific to autoimmune bullous disease. Patients with clinically and histologically diagnose autoimmune bullous disease will be recruited and interviewed regarding the ways their disease affects their quality of life. Based on these responses, a pilot questionnaire will be developed and given to 70 patients. Statistical analysis will then be performed based on the results of these questionnaires to determine whether the instrument is statistically sound or not. If it is validated, the instrument can then be used as a tool to measure quality of life in patients with autoimmune blistering skin diseases.
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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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Professor Dedee Murrell
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Address
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Department of Dermatology, St George Hospital, Gray Street, Kogarah, NSW, 2217
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Country
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Australia
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Phone
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+61-2-9113-2543
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Fax
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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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Professor Dedee Murrell
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Address
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Department of Dermatology, St George Hospital, Gray Street, Kogarah, NSW, 2217
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Country
8586
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Australia
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Phone
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61-2-9113-2543
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Fax
8586
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Email
8586
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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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