Your voice in the tumor board: study tests if patient reports lead to better cancer treatment

NCT ID NCT07671937

First seen Jun 27, 2026 · Last updated Jul 02, 2026 · Updated 1 time

Summary

This study will include about 2,748 people with breast, gynecologic, or pancreatic cancer. Researchers want to see if adding patient-reported outcomes—like symptoms, preferences, and travel distance—to tumor board discussions helps doctors make better treatment decisions. The goal is to reduce treatment delays and side effects while improving patient experience.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance
patient-reported outcomes (ePROs) integrated into tumor board discussions
What this could lead to
If successful, this could show that including patient feedback in treatment planning leads to better-tailored cancer care and fewer treatment side effects.
What could go wrong
This is an early-stage behavioral study, not a drug trial. It may not change actual treatment outcomes, and results may vary across different hospitals.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • University of Alabama at Birmingham

    Birmingham, Alabama, 35294, United States

  • University of California Los Angeles (UCLA)

    Los Angeles, California, 90404, United States

  • University of Oklahoma (OU) Health Campus

    Oklahoma City, Oklahoma, 73126-0901, United States

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