Controlled Interventional Clinical Study Sub-Task

A Controlled Interventional Clinical Study Sub-Task is a inteventional clinical study sub-task within a clinical trial.

• Context:
  • It can be referenced in a Clinical Trial Process.
  • It can range from being a Phase I Clinical Trial Sub-Task (for a phase-1 CT), Phase II Clinical Trial Sub-Task, Phase III Clinical Trial Sub-Task, Phase IV Clinical Trial Sub-Task.
  • It can include: Patient Recruitment (and be represented within a clinical trial process model).
  • …
• Example(s):
  • Clinical Trial Protocol Document Creation Task (to create a clinical trial protocol).
  • Clinical Trial Site Selection & Initiation Task.
  • Clinical Trial Participant Recruiment & Enrollment Task, composed of clinical trial recruitment, clinical trial screening, clinical trial consenting, ...
  • Clinical Trial Study Execution Task.
  • Clinical Trial Data Analysis Task.
  • Clinical Trial Study Report Creation Task (to create a clinical study report).
  • …
• Counter-Example(s):
  • an Observational Clinical Study Sub-Task.
• See: Clinical Trial Management System, Clinical Trial Phase.

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