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Cancer center directors, trial submitters, principal investigators, and other trusted sources must request access to the Accrual application in order to record subject accrual information. They can request access by contacting their organization's site admin or the CTRO. In your role as abstractor, you can grant or deny registered users access to Accrual on a per-participating site basis. One user may request access to more than one trial and to more than one participating site. Similarly, more than one Accrual user can access a given trial and a given participating site.

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Requirements for granting/denying access include the following:

  • Processing status – Must be at least "Verified" (response or no response). See Trial Processing Statuses.
  • Site recruitment status – Must not be "Withdrawn" nor "Not yet Recruiting". The participating site must have accrued patients at some point in the past, or is accruing patients currently.
  • Action – You can grant or deny access to the Accrual site only when abstracting or validating the trial for which access is requested.

Once assigned, users can submit accrual data for all trials associated with their affiliated organization or organization family members. For Complete trials (Institutional and Externally Peer Reviewed), the organization must be a lead; for Abbreviated trials (Institutional), the organization must be a participating site.

Assignment at the organization or family member organization level pertains to trials that the organization has registered in CTRP and extends to those that it will register in the future.

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Complete trials for which the assigner's organization is the lead organization

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Abbreviated trials for which the assigner's organization is the Lead Organization or participating site

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  • By trial
  • By Organization
  • By Organization Family member

    Footnote

    The system automatically assigns the Organization Family Accrual Submitter access to any trial registered by new organizations added to an organization family in the future.  It withdraws access if the Organization Family Accrual Submitter's organization is removed from the organization family in the future.

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  • By trial
  • By participating site

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  • All Complete trials registered by the submitter's organization or family member organization
  • Trials currently registered in CTRP
  • Trials that the organization registers in CTRP in the future, once abstracted

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  • All abbreviated trials registered by the submitter's participating site only
  • Trials currently registered in CTRP
  • Trials that the organization registers in CTRP in the future, once abstracted

Accrual Access Requirements and Rules

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Setting Up Accrual Access

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Activating and Inactivating Accrual Access

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Setting Up Accrual Access

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When you receive a CTRO request for access, you must associate the user with the appropriate trial/site. Thereafter you can grant or deny the user access without having to repeat the setup.

Organization Administrators assign Accrual access in CTRP Registration. However, you still can use this feature in the Protocol Abstraction application to process requests that have been sent to the CTRO.

How to Manage Accrual Access

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Search for the trial of interest. For instructions, refer to Searching for Trials in PA.

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In the search results, click the NCI Trial Identifier link for that trial. The Trial Identification page appears.

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On the Trial Identification page, check out the trial for Administrative processing. For instructions, refer to Checking In and Checking Out Trials. (This checkout step is optional for Super Abstractors.)

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In the various fields, specify the appropriate information. The following table describes the fields. An asterisk (*) indicates a required field.

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Trial Description

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Instruction

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User Name

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Select the appropriate registered user from the drop-down list.
The user’s email address and phone number fields are populated automatically.

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Accessing Site

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Select the appropriate participating site. The Site Recruitment Status field is populated automatically.

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Access Status

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Select either Active, to grant access, or Inactive, to deny access.

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Request Details

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Optionally, type the details of the request as recorded by the CTRO.

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Activating and Inactivating Accrual Access

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Once a user has been set up for a given trial/site, you can grant (Activate) or deny/revoke (Inactivate) the user’s access.

How to Activate and Inactivate Accrual Access

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Search for the trial of interest. For instructions, refer to Searching for Trials in PA.

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In the search results, click the NCI Trial Identifier link for that trial. The Trial Identification page appears.

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On the Trial Identification page, check out the trial for Administrative processing. For instructions, refer to Checking In and Checking Out Trials. (This checkout step is optional for Super Abstractors.)

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