Welcome to the Maternal & Perinatal Central Coordinating Research Hub (CCRH), a coordinating centre for maternal and perinatal research, hosted by the Liggins Institute and supporting the ON TRACK Network. In collaboration with the Department of Obstetrics and Gynecology, and Department of Paediatrics: Child and Youth Health, University of Auckland.
Click here for an overview of CCRH Services & Support. Contact: researchhub@auckland.ac.nz
CCRH Guides
- Planning a Trial
- Study Protocol
- Participant Information and Consent
- Standard Operating Procedures
- Trial Committees
- Authorship
- Data Sharing
- Māori Responsiveness
Randomisation
- CCRH Randomisation Site
- CCRH Randomisation Demo (code:991000tst)
- CCRH Study Numbers
- Randomisation Plans
Data Management
- REDCap FMHS
- REDCap Resources
- Variable Naming Conventions
- Study Reports (Use Edge, Firefox or Chrome)
Analysis
- Normal distribution calculator
- OpenEpi - open source statistics
- SAS Tips
- NZDep2013 Index of Deprivation
- Trial Analysis
- Data Cleaning
Follow-up
- Bayley Scales Age Calculator
- LifePath Follow-up SharePoint
- NZ Travel Calculator
- Definitions for Follow-up Studies
CCRH Admin
- Redmine
- CCRH SharePoint (use IE for file management)
- Creating REDCap Accounts
- Liggins VPN Access
- University of Auckland Staff Intranet
- Space statistics
Consensus Statements and Checklists
Protocols
Outcomes
Reporting
- CONSORT 2010 - Reporting Parallel Group RCTs
- CONSORT 2010 - Extension to Cluster RCTs
- CONSORT 2010 - Extension to Noninferiority / Equivalence RCTs
- StRONNG Checklist - Reporting of Neonatal Nutrition and Growth
- STROBE Statement - Reporting Observational Studies
- STROBE Statement - Explanation & Elaboration
- STARD 2015 - Diagnostic Accuracy Studies
- TIDieR Checklist - Reporting of Interventions
- Very Preterm Birth Studies (Pediatrics 2016)
Analysis
Data Monitoring
- DAMOCLES - Charter for Clinical Trial Data Monitoring Committees
- ERCIN 2011 - Standards Requirements for GCP-Compliant Data Management in Multinational Clinical Trials
Synthesis & Translation
- PRISMA-P 2015 - Preferred Reporting for Systematic Review and Meta-analysis Protocols
- PRISMA 2009 - Preferred Reporting Items for Systematic Reviews and Meta-analyses
- PRISMA-IPD 2015 - Preferred Reporting Items for a Systematic Review and Meta-analysis of Individual Participant Data
- PRISMA Extension 2015 - Network Meta-analyses
- PRISMA-C Extension 2016 - Systematic Reviews and Meta-analyses of Newborn and Child Health Research
- MOOSE - Reporting of Meta-analysis of Observational Studies in Epidemiology
- GRADE - Grading Quality of Evidence and Strength of Recommendations
- AGREE II - Assessing Quality and Reporting of Practice Guidelines
- PROSPERO Registration of Systematic Reviews - Checklist
- ROBINS-I - Risk of Bias In Non-randomized Studies of Interventions
- CRRH template for SR of association
Laboratory
Training
- NIH Protecting Human Subjects certificate
- NIH GCP course
- ROCHE GCP course
- Cultural Competency
- Infection control
- ON TRACK Trial Development Workshop 2018
- Defining research, audit and evaluation
Key Links
ANZ
- Australia & New Zealand Clinical Trials Register (ANZCTR)
- Health and Disability Ethics Committees NZ (HDEC)
- Health Research Council NZ (HRC)
- IMPACT Clinical Trials Network
- MedSafe NZ
- Neonatal Unit Contacts NZ
- ANZNN Directory
- Online Forms NZ (HDEC / SCOTT)
- Research Offices NZ
- Therapeutic Goods Agency (TGA) Australia