Contribute Data
Step 1
Please check the boxes corresponding to the format of your data.
Please provide contact details for the Principal Investigator who will represent the trial on the VISTA-Prevention Steering Committee:
Please provide contact details for the Principal Investigator who will represent the trial on the VISTA-Prevention Steering Committee:
Please detail the inclusion of relevant documents for your clinical dataset in the check-box below and attach these documents using the file transfer link that will be sent separately.
Terms And Conditions
Prof. Hans Christoph Diener, (VISTA-Prevention Chair)
Department of Neurology
University of Duisburg-Essen
vista.prevention@glasgow.ac.uk
Data Contribution Form
Clinical datasets will be lodged with the Robertson Centre for Biostatistics, University of Glasgow on behalf of VISTA.
Section 1.0 Clinical Dataset Information
Section 1.1
Using the checklist below, please ensure that your clinical datasets meet the eligibility criteria for VISTA-Prevention.
Data Format
Investigator Details
All fields marked with * are essential - Please tick all files that are attached electronically
Memorandum of Understanding Summary
- Clinical data will be stored by the Robertson Centre for Biostatistics, University of Glasgow, on behalf of VISTA.
- Clinical datasets should be accompanied by an annotated Case Report Form which explains variable names and codes.
- Contribution of trial data to VISTA entitles the principal investigator to a seat on the VISTA Steering Committee. In this role they will be responsible for the review of proposed projects using the VISTA resource and the approval of subsequent manuscripts for publication.
- All abstracts or manuscripts will be reviewed by the Steering Committee prior to submission for publication. This applies to both national and international publications.
- Analyses will not be undertaken and/or published or reported to an outside group without the knowledge and approval of the VISTA Steering Committee.
- Analyses based on individual trials will not be granted without prior consent by the PI for the named trial/ registry.
- Inadvertent un-blinding of any individual study in an internal report may not be perpetuated in any subsequent publication.
- Any publication arising through VISTA analyses will be accompanied by an acknowledgement that the study is a part of the VISTA Collaboration.
- Contributing trialists whose anonymised data are used in analyses will be offered co-authorship of subsequent manuscripts, provided that authorship criteria are met.
I hereby acknowledge that I have read and understood the terms and conditions and consent to the contribution of the proposed trial/ registry to VISTA.
The raw datasets can be transferred using the University of Glasgow’s file transfer system. A separate link will be emailed to you following submission of this form.