UPCC 04024 Effect of Automated Monitoring for Patients with Imaging Findings of Possible Abdominal Cancer

Enrolling By Invitation
99 years or below
All
Phase N/A
18000 participants needed
1 Location

Brief description of study

To determine the effect of provider contact on clinically-indicated follow-up for imaging findings potentially representing cancer. Our primary variable is 1) rates of clinically indicated imaging and pathology follow-up completed within recommended time interval, before contacting the provider and 2) rates of clinically-indicated follow-up completed after the recommended time interval, after contacting the provider. Our secondary outcome variable is utilization of abdominal imaging and biopsy/surgery associated with potential imaging findings of cancer before and after provider contact (Appendix A). We focus on this downstream utilization because of the importance of this outcome in assessing comparative effectiveness of automated monitoring. In addition, we will measure overall utilization and costs of diagnostic tests and procedures before and after provider contact.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Medical Research
  • Age: 99 years or below
  • Gender: All

TBD

Updated on 22 Apr 2026. Study ID: 17-0267
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Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.

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