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Trial registered on ANZCTR
Registration number
ACTRN12613000325707
Ethics application status
Approved
Date submitted
29/11/2012
Date registered
25/03/2013
Date last updated
19/10/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Waitemata Community Wellness Biobank: analysis of stored biological samples to evaluate health outcomes and plan public health strategies
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Scientific title
Waitemata Community Wellness Biobank: analysis of stored biological samples to evaluate health outcomes and plan public health strategies
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Secondary ID [1]
281603
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Nil
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Universal Trial Number (UTN)
U1111-1137-4472
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Trial acronym
NSH Biobank
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cardiovascular disease
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Diabetes
288677
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Obesity and metabolic disease
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Gastrointestinal cancer
288679
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Condition category
Condition code
Cardiovascular
288261
288261
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0
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Diseases of the vasculature and circulation including the lymphatic system
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Diet and Nutrition
288262
288262
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0
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Obesity
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Metabolic and Endocrine
288263
288263
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0
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Diabetes
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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 an observation of the exposure of an individual to current medical standard of care e.g. current medicines etc and environmental exposure e.g. diet and smoking. This exposure will be compared with long-term health outcomes using electronic medical records and coded DRGs. Genomic DNA from whole blood and plasma will be stored on patients. Genomic, proteomic and metabolomic analysis will be applied to the samples to assess interactions between the individual, drugs and environment. Data will also be aggregated from electronic clinical records and patient questionnaires. The patient questionnaire will be completed at the beginning of the study and will not be repeated. Blood samples will be collected at 6mths, 1, 2, 3, 5 and 10 year periods.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
The historical control will be the baseline results for the same patient if the patient represents to hospital or clinic and has further blood drawn. Alternatively the historical control will be patients treated in the past with older treatment practices.
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Control group
Historical
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Outcomes
Primary outcome [1]
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Incidence of cardiovascular disease as assessed using data linkage to electronic medical records
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Assessment method [1]
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Timepoint [1]
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6 months, 12 months, 2 years, 3 years, 5 years, 10 years. Participants will not necessarily be recalled. Outcomes will be assessed using electronic medical records.
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Secondary outcome [1]
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Incidence of diabetes complications and control using the HBA1C assay
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Assessment method [1]
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Timepoint [1]
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6mths, 12mths, 2yrs, 3yrs, 5yrs, 10yrs
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Secondary outcome [2]
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Incidence of gastrointestinal cancer assessed through colonoscopy results in electronic medical records, and ICD10 diagnosis codes.
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Assessment method [2]
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Timepoint [2]
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6mths, 12mths, 2yrs, 3yrs, 5yrs, 10yrs
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Secondary outcome [3]
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Incidence of inflammatory bowel disease using inflammatory markers, patient diary and/or electronic medical records.
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Assessment method [3]
301915
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Timepoint [3]
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6mths, 12mths, 2yrs. 3yrs, 5yrs, 10yrs
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Eligibility
Key inclusion criteria
Patients presenting to hospital via ambulatory clinics or the emergency department. Community patients from primary care will also be included.
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Minimum age
16
Years
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Maximum age
110
Years
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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
Nil
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Case control
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Timing
Both
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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
1/04/2013
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Actual
5/05/2015
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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
5000
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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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New Zealand
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State/province [1]
4697
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Theranostics Lab
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Address [1]
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26 Volcanic St,
Mt Eden,
Auckland 1041
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Country [1]
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New Zealand
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Primary sponsor type
Hospital
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Name
North Shore hospital
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Address
124 Shakespeare Rd, Westlake 0622, New Zealand
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Country
New Zealand
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Secondary sponsor category [1]
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Charities/Societies/Foundations
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Name [1]
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New Zealand Institute of Clinical Excellence
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Address [1]
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North Shore hospital clinical laboratory,
Shakespeare Rd,
Takapuna,
Auckland 0622
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Country [1]
285196
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
288489
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Northern A Regional Ethics Committee
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Ethics committee address [1]
288489
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Ministry of Health No 1 The Terrace PO Box 5013 Wellington 6145
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
288489
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04/12/2012
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Approval date [1]
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01/04/2015
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Ethics approval number [1]
288489
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Summary
Brief summary
This resource/biobank has two main aims. The first aim is to gain a better understanding of the interactions between genes, environment and the way we live that influence health or cause diseases. The second aim is to use this understanding to develop new drugs, genetic tests and treatments and to plan public health strategies.
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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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Dr Patrick A. Gladding
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Address
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26 Volcanic St,
Mt. Eden,
Auckland 1041
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Country
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New Zealand
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Phone
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+64220424325
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Patrick A. Gladding
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Address
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26 Volcanic St,
Mt Eden
Auckland 1041
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Country
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New Zealand
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Phone
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+64220424325
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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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Patrick Gladding
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Address
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26 Volcanic St,
Mt Eden
Auckland 1041
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Country
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New Zealand
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Phone
9172
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+64220424325
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Fax
9172
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Email
9172
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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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