Enable and disable ePRO for participants in Study Connect.
Note Veeva ePRO is only available to sites whose sponsors are using Veeva ePRO in Clinical Operations.
Overview
You can enable ePRO for participants in Study Connect to allow them to receive surveys and notifications in MyVeeva for Patients on their own device or on a provided device.
Prerequisites
In order to enable a participant with ePRO, the following prerequisites must be met:
- Study Invitation: Your study’s sponsor must be using Veeva ePRO and your site administrator must have accepted the sponsor’s study invitation. See the Connecting Your Study to ePRO help topic for more information.
- Participant: A participant record must exist. If the participant record contains an email address and a phone number, the user can register a MyVeeva account with that information. If the participant record doesn’t contain an email address and/or phone number, you can create a Device Registration Code (DRC) that they can use to register an account. See the Managing Study Participants in Study Connect help topic for more information on creating or updating participant records.
Enabling ePRO for a Participant
Enabling ePRO for a participant means they can be assigned the study’s ePRO schedules, receive survey tasks, and be notified of their available, due, and missed surveys. When you enable a participant with ePRO in Study Connect, they take their surveys in the MyVeeva for Patients application. See the Surveys help topic in MyVeeva for Patients Help for more information.
Each participant must be enabled with ePRO to participate in a Veeva ePRO study. Surveys or survey-related notifications may not appear for the participant until you enter the dates and times for their participant events. See the Managing Participant Event Dates and Times help topic for more information.
To enable ePRO for a participant, complete the following steps:
- In Study Connect, select Surveys on the left menu.
- Select the Participants tab.
- On the Participants page, select the participant beneath the Patient Name column.
- Locate the ePRO Status field and select Enable.
- On the Enable ePRO pop-up, select Enable. When complete, you’ll receive a notification. This process may take a few minutes.
Once enabled, participants receive a welcome email with instructions for registering a MyVeeva for Patients account. Participants must register or already have a registered account in the MyVeeva for Patients application to begin taking surveys. If a participant needs help registering a MyVeeva for Patients account or managing their surveys in MyVeeva, see the Registration and Login and Surveys help topics in MyVeeva for Patients Help.
After a participant is enabled with ePRO, all relevant participant events for the study are automatically created for them under the participant events section on the participant’s page in Study Connect.
Any schedules or notifications related to the assigned events begin or send as soon as a participant is enabled with ePRO.
Disabling ePRO for a Participant
Disabling ePRO for a participant means they’re no longer assigned your study’s survey schedules and no longer receive surveys and notifications.
To disable ePRO for a participant, complete the following steps:
- In Study Connect, select Surveys on the left menu.
- Select the Participants tab.
- On the Participants page, select the participant beneath the Patient Name column.
- On the participant’s page, select Disable ePRO from the all actions menu (
). There may be a delay of a few minutes while ePRO is disabled for the participant, and you receive a notification when it’s complete.