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Category: Project

Description: This project can be used as a template to guide clinical research collaborative studies on their use of the OSF. The OSF should not be used to store sensitive data and protected health information but is ideal for sharing non-sensitive materials such as study protocols and consent forms (unsigned).

License: CC-By Attribution 4.0 International

Model clinical research project | Discussion

Wiki

How to use the OSF to manage a clinical research workflow

  1. Create Components to store and share non-sensitive clinical research materials. For example, create separate components for:

    a. protocol materials and study design information,

    b. consent forms (unsigned),

    c. analysis plans and scripts from your statistician,

    d. IRB forms and information.

  2. Add your team to those components that they need…

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Citation

Components

Protocol


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Consent form


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Analysis


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IRB forms


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clinical trialIRBprotocol

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