Setting the blind logic in the trial

This guide outlines a straightforward process for setting up blinding logic in a clinical trial to ensure trial integrity. By following the instructions below, users can easily navigate the system to configure blinding settings, which is crucial for obtaining objective results. Understanding and effectively implementing these settings is essential for investigators and study coordinators to maintain the validity of their studies.

Hyggio Support
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7 steps
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26 seconds

Hyggio

Navigate to [Trial->settings](https://app.sit.hyggio.com/clinical-trial/trial/11191/settings?active_step=ESOURCE)

Click "eSource"

Tip!\ In the Hyggio system, we introduced two approaches to blinding.\ **Not applicable** — no blinding is applied; all study team members can view every part of a visit, subject to their permissions.\ **Blinded / Unblinded** — blinding is enforced; selected team members see only the elements allowed by their blinding status. For example, if a user is **unblinded** and a procedure is **blinded**, the user will not see the entered values for that visit item.

Select Data blinding

Click "Save"

Click "Team"

Click "User"

Click "Blinded"

When the blinding configuration is changed in an ongoing study, all study team members must update and confirm their correct blinding status after the edit. Likewise, if the change affects existing procedures or fields, the system will require users to adjust the blinding settings for those items during editing!