The proposed research will contain data from approximately 500 subjects who will be examined at a downtown stD clinic for three sexually transmitted (STD) bacterial diseases. The final dataset will include demographic and behavioural data provided by interviewees and laboratory data from urine samples. Since the STDums examined are notifiable diseases, we will collect identifying information. Even if the final dataset is deleted prior to publication for the release of identifiers, we believe that there is still the possibility of deductive disclosure of subjects with unusual properties. Therefore, we only make the data and documents associated with users available as part of a data-sharing agreement that provides: (1) the obligation to use the data solely for research purposes and not to identify a single participant; (2) obligation to secure data with appropriate computer technology; and (3) the obligation to destroy or return the data at the end of the analysis. These guidelines contain the National Institutes of Health(NIH) policy statement on data exchange and additional information on the implementation of this policy. Sharing the data generated in this project is an essential part of our proposed activities and takes place in different ways. We want to make our findings available to the community of scientists interested in [this disease] and the biology [of their agent] to avoid involuntary double research. Conversely, we would appreciate working with others who could use the vaccination assessment protocols developed in the [project]. Data Enclave – A controlled and secure environment in which legitimate researchers can perform analyses with limited data resources. Scientific authors should recognize the source of the data on the basis of which their manuscript is based. Many investigators record this information in the methods and/or reference sections of their manuscripts. Newspapers usually contain a confirmation section in which authors can identify the people who helped them access the data.
Authors using shared data should check the policies of the journal to which they wish to make themselves available to determine the exact location of the manuscript for such confirmation. Most magazines now believe that the DNA and amino acid sequences that appear in articles will be presented before the publication of a sequence database. Punctuality – In general, NIH believes that the publication and sharing of data in a timely manner is, at the latest, the acceptance of the publication of the main results of the final data set. However, real time is influenced by the nature of the data collected. Researchers seeking NIH support for clinical trials may wish to consider several factors when developing their data exchange plan. Researchers who wish to plan clinical trials and share the data obtained should be carefully informed before the start of the study on the design of the study, the informed consent documents and the structure of the resulting data set. For example, many clinical trials use small samples at an early stage, making it difficult to protect participants` privacy.