Evaluating a Virtual Oncology Program for Veterans with Cancer

Evaluating the Implementation of a Comprehensive Multilevel Virtual Oncology Program Among Veterans Diagnosed With Lung, Colorectal, Prostate, and Breast Cancers in the US Department of Veterans Affairs

Observational NYU Langone Health · NCT06559059

This study is testing a virtual cancer care program for veterans to see if it helps them get better treatment and support for lung, colorectal, prostate, and breast cancers.

Quick facts

Study typeObservational
Enrollment1800 (estimated)
Ages18 Years and up
SexAll
SponsorNYU Langone Health Academic / other
Locations5 sites (Brooklyn, New York and 4 other locations)
Trial IDNCT06559059 on ClinicalTrials.gov

What this trial studies

This observational study aims to assess the effectiveness of the VA National TeleOncology program, a telehealth initiative designed to improve cancer care for veterans diagnosed with lung, colorectal, prostate, and breast cancers. By utilizing the Veterans Health Information Systems and Technology Architecture (VistA), the study will identify eligible patients and analyze their telehealth engagement, clinical quality, and healthcare costs. The focus is on understanding how social determinants affect telehealth access and outcomes, ultimately promoting health equity among veterans.

Who should consider this trial

Good fit: Ideal candidates include veterans aged 18 and older who have been newly diagnosed with lung, prostate, breast, or colon cancer within three months of their telemedicine visit.

Not a fit: Patients who have not engaged with VA providers in the past year or those with a prior diagnosis of the specified cancers will not benefit from this study.

Why it matters

Potential benefit: If successful, this program could enhance cancer care delivery and accessibility for veterans, leading to improved health outcomes.

How similar studies have performed: Other studies have shown promising results with telehealth interventions in oncology, indicating potential for success in this approach.

Eligibility criteria

Show full inclusion / exclusion criteria
Patients Inclusion Criteria:

1. A Veteran
2. Aged 18 years or older
3. Newly diagnosed with lung, prostate, breast, or colon cancer within 3 months of telemedicine visit
4. Engaged in an oncology visit during the 36-month analysis period at a Veterans Affairs Medical Center (VAMC) location.

VAMC Providers and Staff Inclusion Criteria:

1. Provider or staff member at one of the VAMC locations including physicians, nurse practitioners, physicians' assistants, and nurses caring for Veterans
2. Providers or staff members having helped provide care for at least 5 Veterans with cancer in the previous 6 months at a VAMC location

Patients Exclusion Criteria:

1. Veterans who have not seen any providers in the VA within the past year
2. Patients previously diagnosed with lung, prostate, breast, or colon cancer
3. Pregnant patients

VAMC Providers and Staff Exclusion Criteria:

1\. Providers or staff members who do not help treat Veterans with specified cancers in oncology at the VA

Where this trial is running

Brooklyn, New York and 4 other locations

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Lung Cancer DiagnosisColorectal CancerProstate Cancer DiagnosisBreast Cancer Diagnosis
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.