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Trial registered on ANZCTR
Registration number
ACTRN12609000786291
Ethics application status
Approved
Date submitted
2/09/2009
Date registered
9/09/2009
Date last updated
9/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Health-related quality of life and illness perception in colorectal surgery
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Scientific title
Health-related quality of life and illness perception in colorectal surgery
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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:
Colorectal disease
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Condition category
Condition code
Surgery
239915
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0
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Other surgery
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Oral and Gastrointestinal
239963
239963
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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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
This is not an interventional trial. This is a validation study of a novel quality of life too. Participant will complete quality of life tools before surgery and day 2, 7 and 14 post-operative. This study will run over a 2 year period.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
There is no control group.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Construct validity and responsiveness of the ASIS (abdominal surgery impact scale) in patients undergoing elective major colorectal surgery. The ASIS will be correlated to 1) SF-36 Acute (one week recall version of the short form 36 generic quality of life instrument) and 2) symptom scores (self-rated pain, fatigue etc on 0-10 scales). Total scores will be compared, as well as subscales (overall score, physical limitations, functional impairment, pain, visceral function, sleep and psychological function).
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Assessment method [1]
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Timepoint [1]
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Pre-operative, Day 2, 7 and 14 post operative.
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Secondary outcome [1]
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Preoperative stress and illness perceptions. The ASIS will be correlated to 1) SF-36 Acute (one week recall version of the short form 36 generic quality of life instrument) and 2) symptom scores (self-rated pain, fatigue etc on 0-10 scales). Total scores will be compared, as well as subscales (overall score, physical limitations, functional impairment, pain, visceral function, sleep and psychological function).
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Assessment method [1]
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Timepoint [1]
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Pre-operative
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Eligibility
Key inclusion criteria
Patients undergoing elective colorectal surgery at Waitemata District Health Board.
Fluent English speakers and writers.
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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
Patients under the age of 18 years, have
a diagnosed learning disability, or are undergoing a palliative procedure are excluded.
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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
Recruiting
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Date of first participant enrolment
Anticipated
31/08/2009
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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
500
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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0
New Zealand
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State/province [1]
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Auckland
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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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Waitemata District Health Board
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Address [1]
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Dept of Surgery
Waitemata District Health Board
Private Bag 93 503
Takapuna
Auckland 0740
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Country [1]
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New Zealand
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Funding source category [2]
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University
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Name [2]
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University of Auckland
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Address [2]
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Faculty of Medical and Health Sciences
Private Bag 92 019
Auckland 1023
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Country [2]
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New Zealand
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Primary sponsor type
Individual
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Name
Mr Mattias Soop
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Address
Dept of Surgery
North Shore Hospital
Private Bag 93 503
Takapuna
Auckland 0740
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Country
New Zealand
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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 Auckland
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Address [1]
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Faculty of Medical and Health Sciences
Private Bag 92 019
Auckland 1023
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Country [1]
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Northern Y Regional Ethics Committee
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Ethics committee address [1]
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3rd Floor, BNZ Building 354 Victoria St PO Box 1031 Hamilton 3204
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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18/06/2009
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Approval date [1]
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17/07/2009
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Ethics approval number [1]
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NTY/09/42/EXP
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Summary
Brief summary
This study aims to validate the ASIS (Abdominal Surgery Impact Scale) instrument in patients undergoing surgery for colorectal disease. We would like to prove that the ASIS has acceptable validity and responsiveness in colorectal surgical patients. The recruitment goal is 500 patients and the study will be offered to all elective patients having colorectal surgery at Waitemata District Health Board. Patients will be given quality of life questionnaires to complete pre-operatively and then postoperatively on days 2, 7 and 14.
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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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Lauren Porten
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Address
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Dept of Surgery
North Shore Hospital
Private Bag 93 503
Takapuna
Auckland 0740
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Country
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New Zealand
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Phone
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+64 9 486 8920 extn 7125
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Fax
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+64 9 488 4664
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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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Mr Mattias Soop
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Address
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Dept of Surgery
North Shore Hospital
Private Bag 93 503
Takapuna
Auckland 0740
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Country
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New Zealand
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Phone
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+64 9 486 8920 extn 2459
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Fax
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+64 9 488 4664
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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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