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Trial registered on ANZCTR
Registration number
ACTRN12611000446965
Ethics application status
Approved
Date submitted
2/05/2011
Date registered
2/05/2011
Date last updated
2/05/2011
Type of registration
Prospectively registered
Titles & IDs
Public title
Impact of choice of feeding on DNA damage in 3-6 month old infants – a pilot study
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Scientific title
Impact of choice of feeding on DNA damage in 3-6 month old infants – a pilot study
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Secondary ID [1]
260089
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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:
Diet and Nutrition .The aim of the study is to determine whether the choice of how an infant is fed affects their DNA and folate in the body.
265773
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Condition category
Condition code
Diet and Nutrition
252289
252289
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0
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Other diet and nutrition disorders
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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
The collection of a heel prick blood sample from infants when they at 3months of age and then when they are at 6 months of age.Completion of questionnaires relating to health and lifestyle of both the mother and child which includes the feeding regime of the infant will be done twice,when the child is 3 months of age and at 6 months of age.
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Intervention code [1]
264510
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Lifestyle
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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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To determine whether the choice of how an infant is fed affects their DNA and folate in the body.This will be done by collecting the heel prick blood sample from the infants and collecting a feeding and food questionnaire from the mother.The validated Cancer Council of Victoria Food frequency questionnaire will be used.
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Assessment method [1]
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Timepoint [1]
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The mother and infant will attend one visit when the child is 3 months of age and one visit when they are 6 months of age.
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Secondary outcome [1]
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Nil
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Assessment method [1]
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Timepoint [1]
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Nil
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Eligibility
Key inclusion criteria
Healthy mothers and their infants,born at term or at least a minimum of 38 weeks gestation.
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Minimum age
3
Months
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Maximum age
6
Months
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Infants of multiple parity,mothers who cannot understand the study protocol and are unable to give appropriate consent to all stages of the protocol and attend the clinic when the infant is approximately 3 months and 6 months of age.Infants who have been introduced to solid foods prior to 3months of age.
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Both
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
16/05/2011
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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
120
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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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Other Collaborative groups
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Name [1]
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Cancer Council of Australia
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Address [1]
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202 Greenhill Rd
Eastwood SA 5063
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Country [1]
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Australia
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Primary sponsor type
Other Collaborative groups
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Name
Cancer Council of Australia
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Address
202 Greenhill Rd
Eastwood SA 5063
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Nil
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Address [1]
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Nil
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Country [1]
264084
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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 Nathan O'Callaghan
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Address
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Commonwealth Scientific and Industrial Research Organisation
Kintore Ave
Adelaide SA 5000
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Country
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Australia
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Phone
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+61 08 83038867
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Fax
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Email
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Nathan.o'
[email protected]
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Contact person for scientific queries
Name
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Dr Nathan O'Callaghan
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Address
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Commonwealth Scientific and Industrial Research Organisation
Kintore Ave
Adelaide SA 5000
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Country
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Australia
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Phone
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+61 08 83038867
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Fax
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Email
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Nathan.o'
[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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