Improving Precision Oncology for Lung and Prostate Cancers

This study is testing a "Multilevel Intervention" to improve how often patients with advanced lung or prostate cancer at VA medical centers receive precision oncology (PO). PO uses molecular testing to find specific changes in a tumor that can be treated with targeted therapy. The intervention has three parts: a short educational video for patients, feedback to doctors about their PO practices, and changes to the electronic medical record to make ordering and reviewing PO tests easier. The study aims to see if these changes increase the use of molecular testing over three years. You may be able to join if you are a veteran with advanced lung or prostate cancer being seen at a VA oncology clinic. The study is currently unclear on its recruitment status.

Study design
This interventional study plans to include 2653 participants. It is testing a multilevel intervention with three components.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary goal of the study will be measured at 3 years, which suggests a follow-up period of at least that long.

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NCT06825715

Multilevel Intervention for Precision Oncology

Recruiting
NAAll AgesInterventionalHealth services
VA Office of Research and Development
~2,653 participants
Updated 2026-07-07 on ClinicalTrials.gov
What's tested:Multilevel intervention

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Use of molecular testing
Measured over 3 years
Advanced Cancers of the Prostate
Cancers of the Lung
1 sites across 1 states
New York1
  • Daniel J Becker, MD · PRINCIPAL_INVESTIGATOR · VA NY Harbor Healthcare System, New York, NY

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Eligibility criteria

Inclusion

Patients in the VA with cancer of the lung or prostate who are seen in the oncology clinic

Exclusion

Cancer that did not originate in the prostate or the lung
  • Use of molecular testing3 years

    Proportion of eligible patients with lung and prostate cancer who have next generation sequencing molecular testing