NVDRS Data Access
NVDRS data are stored in an incident-based, relational database. Descriptive data can be accessed free of charge from NCIPC’s Web-based Injury Statistics and Query System (WISQARS). More detailed data from the NVDRS Restricted Access Database (RAD) are available by request for users meeting certain eligibility criteria.
WISQARS Violent Deaths (NVDRS) Module
WISQARS is an interactive query system that provides data on fatal and nonfatal injuries in the United States. Any data user can access WISQARS online.
The NVDRS module in WISQARS provides descriptive information on violence-related deaths available from participating states. The query system provides incident counts as well as crude and age-adjusted death rates by manner of death and cause of injury. Also, queries can be tailored to include states, years, age ranges, sex, and racial or ethnic groups of interest. Visit WISQARS NVDRS online for more information.
NVDRS Restricted Access Database (RAD)
The NVDRS Restricted Access Database (RAD) is a de-identified, multi-state, case-level data set comprising hundreds of unique variables. The database includes short narratives to describe the circumstances related to violent deaths, including descriptions from law enforcement and medical examiner or coroner investigative reports.
The RAD contains confidential information that could lead to accidental disclosure of the identity of suspects and victims. CDC protects these data by requiring users to meet certain eligibility requirements and to take steps necessary to ensure the security of data, preserve confidentiality, and prevent unauthorized access.
At this time, there are no costs for accessing the NVDRS RAD. It is also important to note that CDC staff are unable to provide analytic or other technical assistance to recipients for the proposed research. Eligible investigators must prepare and submit a proposal. The ability of the principal investigator to conduct the proposed analyses and to comply with NVDRS RAD security, confidentiality, and data protection requirements are considered during the proposal package review process.
Eligibility to Apply for RAD Access
To request access to the NVDRS RAD, the primary investigator must meet all of the following criteria:
- Have a PhD, DrPH, MD, ScD, DO, or another doctoral-level degree
- Hold a research position or faculty appointment at a research organization, government agency, or institution of higher education. This includes research foundations or grant-making organizations.
- Agree to comply with NVDRS RAD security, confidentiality, and data protection requirements, as outlined during the review process
Local, county, state, and federal government employees, regardless of degree or research position, are also eligible to apply for the NVDRS RAD.
Proposal Package and Submission
The 2-4 page proposal package must include the items listed below. Submit the package to NVDRS RAD at firstname.lastname@example.org.
- Cover letter on official home institution letterhead
- Project title
- Abstract: maximum of 250 words summarizing the project
- Full personal identification, institutional affiliation, mailing addresses, phone, and email address of the person to be primarily responsible for the care of the data and for compliance with the terms of the data sharing agreement
- Names of all other collaborators who will be accessing the RAD files under the principal investigator’s supervision
- Source of funding for the proposed project, if applicable
- Background of study (maximum of 250 words):
- Key study questions or hypotheses
- Public health benefits. Requestors must provide evidence of a legitimate public health purpose that justifies the use of the data.
- Methods for the study (maximum 700 words) including:
- Summary of the variables needed for the proposed research. A variable specifications sheet that lists available variables in NVDRS will be provided prior to submitting the proposal and should be used for this purpose. This sheet with requested variables should be returned with the proposal. In addition to specifying the requested NVDRS variables, any data from other sources that might be merged with NVDRS data should be described. To obtain the NVDRS coding manual and other NVDRS related materials, please visit the NVDRS Technical Assistance page.
- Proposed analytic strategy (e.g., statistical analysis, data linkages).
- Data management plan, including a description of the mechanisms that will be in place to secure the data, preserve confidentiality, and prevent unauthorized access. This plan should include information about data storage, limitations on access to the data, technical security practices in place such as password protection, use of stand-alone computers, encryption, and procedures covering networked computers and servers. This section must also include a description of the destruction of all NVDRS RAD files, and all derived files, when the approved use of the data will have been completed (i.e., on the agreed upon date scheduled by the CDC). The destruction date is five years from the receipt of the data unless otherwise specified.
- Description of the anticipated products, reports, and publications to be derived from the data analyses (max. 250 words).
- Completed and signed copy of the NVDRS Data Sharing Agreement (Note: All collaborators who will be accessing the RAD files under the requesting Principal Investigator’s supervision must sign the NVDRS RAD Data Sharing Agreement.). The NVDRS Data Sharing Agreement form should be requested prior to submitting the proposal.
- Signed copy of approval from the institutional review board, if the proposal includes any potential linking of NVDRS data with another data source that contains personally identifiable information.
The NVDRS RAD review committee consists of a panel of scientific and data analysis experts within CDC’s National Center for Injury Prevention and Control.
Upon receipt of the proposal package, a committee will review the submission to ensure it meets the requirements established to protect the confidentiality of the data. The review committee will assess the following criteria for each proposal:
- Scientific and technical feasibility of the study
- Qualifications of all people who will have access to the data
- Consistency between requested data and study goals
- Description of any additional data that will be linked to NVDRS RAD data
- Anticipated publications or other dissemination of results
- Risk of disclosure of restricted information
- Protections in place to maintain confidentiality of the data
- A legitimate public health purpose will be served by use of the data
The committee reviews proposals as they are received, and typically responds within 3-4 weeks. An incomplete proposal package will be returned upon receipt. The review of complex projects that require extensive communication between NVDRS staff and the applicants may take longer to complete. When a proposal is approved, the principal investigator will be notified by email and will receive the data via FTP (file transfer protocol).
Investigators are permitted to conduct only those analyses that have received approval. RAD requesters can request to add data years and new investigators/staff to an approved project and to modify the scope of the study. Requests to add data years to an existing project that has been approved will be expedited and committee review is not required.
CDC reserves the right to deny or terminate any project at any time when it deems an investigator’s/researcher’s actions may compromise confidentiality or ethical standards of behavior in a research environment. Failure to comply will result in the cancellation of the research activity and exclusion from future research activities using the NVDRS RAD.
Contact the NVDRS RAD team at email@example.com for the following:
- To ask questions and further information about the NVDRS RAD
- To request a copy of the NVDRS RAD data sharing agreement
- To request a copy of the NVDRS RAD variable specification sheet
- To submit the proposal package
- To submit an amendment form (if applicable)