REFLEX Study

The REFLEX Study

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Data Management

Plans for data entry, coding, security, and storage, including any related processes to promote data quality (eg, double data entry; range checks for data values). Reference to where details of data management procedures can be found, if not in the protocol.

Research Data Management Policy document.

  1. Description of the data
    1.1 Type of study
    Unblinded randomised controlled trial, with a nested cost-effectiveness evaluation
    1.2 Types of data
    Quantitative data on participant demographics and health status including liver disease and background
    comorbidities.
    Results of a Markov cost-effectiveness model including incremental cost effectiveness ratios
    1.3 Format and scale of the data
    All data will be collected once from all participants (n=640). Long-term outcomes including incident liver cancer
    and death will be collected from routine health data after completion of the main study in accordance with
    ethical approvals. Data will be entered into an Excel database (double entry) and transferred to SPSS (or like
    databases) for statistical analysis. Databases will be password protected and stored securely on University of
    Southampton computers. The results of statistical analyses will be recorded electronically as SPSS/R/Stata output
    files. The Markov model and its outputs will be designed and stored on as University of Southampton computer.
  2. Data collection/generation
    2.1 Methodologies for data collection/generation
    Data will be collected using validated questionnaires, validated tests for liver cirrhosis and laboratory methods.
    All research will be conducted according to standard operating procedures (SOPs) and all staff will be fully
    trained to assure competence. Any programmatic scripts produced to analyse these data will be made available
    in a public repository (e.g github.com) under an open source licence
    2.2 Data quality and standards
    All laboratory and clinical methods will be performed in accordance with University of Hospital
    Southampton/manufacturer guidance. SOPs will be followed and staff will be trained appropriately. Analyses will
    be conducted in duplicate. A data analysis plan will be developed. Dual entry of data into Excel spreadsheets will
    be used.
  3. Data management, documentation and curation
    3.1 Managing storing and curating data
    Original hard copy data (e.g. questionnaires, consent forms, eligibility screening sheets) will be stored securely in
    a locked cabinet within the University of Southampton in accordance with ethical approvals. Data will be (double)
    entered into Excel spreadsheets on a regular basis; these will be password protected. These spreadsheets will be
    backed up daily on the institutional server. Statistical analysis will be conducted in SPSS or other software where
    more appropriate. Again such spreadsheets will be password protected and backed up.
    3.2 The study will be registered as a clinical trial at www.clinicaltrials.gov. Once the findings from the trial are
    published, the record will be updated to indicate that data are available from the PI upon request. The data will
    be stored on the University of Southampton data repository (http://library.soton.ac.uk/researchdata) and
    approved users will be given access to this. All data will be retained in this repository.
  4. Data security and confidentiality of potentially disclosive information
    4.1 Formal information/data security standards
    The study will be compliant with the University of Southampton Data Protection Policy (May 2018) and the
    General Data Protection Regulation 2016 (Data Protection Act 2018).
    4.2 Main risks to data security
    It is necessary to hold information on subjects’ names and contact details in order to contact them during the
    study. However, such identifiable information will not be stored in any database along with study data. All
    identifiable data will be kept in a password protected electronic file and in hard copy in a locked filing cabinet.
    All data will be linked only to study codes and thus not identifiable with the source subject. However, the caveat
    to this will be a data set recording the subject name and study code without any other subject details.
    All data recorded on paper will be kept in a locked filing cabinet in the researchers’ office and/or in a dedicated,
    restricted access, clinical data storage area (e.g. on Level D of the IDS Building, University of Southampton).
    Data of an identifiable nature (i.e. subject names, contact details, addresses) will be destroyed after the end of
    the project.
    Data will be obtained, handled and stored in adherence to the principles set out in the General Data Protection
    Regulation 2016 (Data Protection Act 2018).
  5. Data sharing and access
    5.1 Suitability for sharing
    We will generate demographic data on ~640 patients with type 2 diabetes. These data are likely to be of interest
    to other researchers.
    5.2 Discovery by potential users of the research data
    Publications from the study and end of study dissemination events (organised by the researchers and PPI
    contributors) will indicate that data are available and how to approach the PI to gain approval for access to the
    data. Once the main findings are published, the study record at www.clinicaltrials.gov will be updated to indicate
    that data are available from the PI upon request. The data, including metadata, will be stored on the University
    of Southampton data repository (http://library.soton.ac.uk/researchdata) and approved users will be given
    access to this.
    5.3 Governance of access
    The data, including metadata, will be stored on the University of Southampton data repository
    (http://library.soton.ac.uk/researchdata). Requests to access the data will be considered in a timely manner by
    the joint-CIs – Ryan M Buchanan & Chris Byrne). Statistical models will be made available in R via GitHub and SBML via model repositories to enable reproduction of the results.
    5.4 The study team’s exclusive use of the data
    We will aim to publish our main findings in a timely manner (e.g. within 6 months of the end of the study). At that
    stage notification of data availability will be widely disseminated through the publication(s) at the time of their
    acceptance for publication.
    5.5 Restrictions or delays to sharing, with planned actions to limit such restrictions
    We do not anticipate such delays because study participants will consent to data sharing prior to study entry. No
    identifiable personal data will be shared. Consequently we do not believe there will be any risk from sharing any
    of the data generated in the study.
  6. Responsibilities
    The co-CIs will have overall responsibility for data management, metadata creation, data security and quality
    assurance of data, Co-Is will each have responsibility for these activities at their sites. The Southampton
    researchers will co-ordinate data management activities among the sites.
  7. Co-funding with industry partners
    Our study is co-funded with Echosens LTD. As per the terms of the contract between UoS and Echosens
    Southampton University have full rights of ownership over the data. Southampton University will collect, store
    and manage the sharing of data generated in this study without hinderance.