Researcher User Personas
|
Background |
HSV research includes all medical research that attempts to prevent, treat or cure herpes, as well as fundamental research about the nature of herpes |
Demographics |
Education: Masters or above |
Identifiers |
Meticulous, require information in the database to be standardised with established governance and oversight plans |
Goals |
Good quality data that is standardised for meta-analysis |
Recruit patients for clinical trials |
Develop therapeutics or learn about population behaviour patterns and their association with disease development |
Improve or monitor health care |
Challenges |
Do not have access to the population of HSV patients for data collection |
Objectives of the registry |
Collect data from HSV patients in a standardised and accurate manner which can be centrally available |
Use Cases
|
Basic flow |
Researchers conduct a literature search on HSV causes and relationships with patient behaviour |
Researchers hypothesize a potential relationship between certain activity and HSV for a certain patient group |
Researchers search the database to search for a certain rate of recurrence for a specific group of patients |
Termination outcome: Researchers use statistical methods to analyse database records to identify potential correlation between patient behaviour and disease |
Alternative flow |
Researchers want to identify certain patient groups for clinical trial recruitment |
Researchers look through a searchable database for patients that fit the clinical trial criteria |
Researchers contact the patients who gave consent. |
Termination outcome: Researchers identify suitable patients quickly |