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GenV Vanguard Cohorts Participant Information Statement and Consent Form

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posted on 04.05.2020 by Melissa Wake, SHARON GOLDFELD, Richard Saffery, William Siero, Danah Hourani, Alisha Gulenc, Libby Hughes

The Generation Victoria (GenV) Vanguard Cohorts Participant Information Statement and Consent Form comprises a 5-page information statement of the purpose, methods, demands, risks and potential benefits of GenV, and a 2-page consent form for completion by parents/guardians. This is version one (dated 17/02/2020), approved by the Royal Children's Hospital Human Research Ethics Committee, and is correct to the best of our knowledge as of May 2020.


We would like to acknowledge the following people for their contributions (in alphabetical order): Katie Allen, Dino Asproloupos, Lynne Atley, David Burgner, Jim Buttery, John Carlin, Jeanie Cheong, Nigel Curtis, Sarah Davies, Ben Edwards, Lottie Gasparini, Harriet Hiscock, Karen Lamb, Joan Leong, Kathryn North, Anne-Louise Ponsonby, Joanne Said, Michael Stringer, and members of the GenV Focus Area and Method Cores Working Groups.


Funding

The Paul Ramsay Foundation

Victorian Department of Health and Human Services

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