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
Conditions
Lung Cancer Diagnosis, Colorectal Cancer (Diagnosis), Prostate Cancer Diagnosis, Breast Cancer DiagnosisSummary
The purpose this pragmatic trial to test the effectiveness of an existing, ongoing clinical service, the VA National TeleOncology program (NTO), a multilevel telehealth population health management program. The primary aims are to study the intervention and determine its effectiveness on telehealth engagement, clinical quality, and healthcare cost outcomes across levels of Social Determinants of TeleHealth (SDTH) with the goal of promoting health equity.
Detailed Description
Study staff will use the Veterans Health Information Systems and Technology Architecture (VistA), the VA health information technology system, to identify eligible patients at VA sites based on listed inclusion and exclusion criteria. Patient records will be observed of Veterans with a new cancer diagnosis of the lung, prostate, breast, or colon and a telehealth visit utilizing the VA National TeleOncology Service (NTO).
Locations
5 locations Found with status Recruiting
Status
- RECRUITING
Central Contacts
- Janeth Juarez Padilla
- 646-501-3588
- [email protected]
Principal Investigator
- Danil Makarov, MD, MHS
Status
- RECRUITING
Central Contacts
- Janeth Juarez Padilla
- 646-501-3588
- [email protected]
Principal Investigator
- Danil Makarov, MD, MHS
Status
- RECRUITING
Central Contacts
- Janeth Juarez Padilla
- 646-501-3588
- [email protected]
Principal Investigator
- Danil Makarov, MD, MHS
Status
- RECRUITING
Central Contacts
- Janeth Juarez Padilla
- 646-501-3588
- [email protected]
Principal Investigator
- Danil Makarov, MD, MHS
Status
- RECRUITING
Central Contacts
- Janeth Juarez Padilla
- 646-501-3588
- [email protected]
Principal Investigator
- Danil Makarov, MD, MHS
Eligibility 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
Study Plan
Veterans
Veterans aged 18 years or older newly diagnosed with lung, colorectal, prostate or breast cancer. Patient records will be observed of Veterans with a new cancer diagnosis of the lung, prostate, breast, or colon and a telehealth visit utilizing the VA National TeleOncology Service (NTO).
VA health care providers and staff members
VA health care providers and staff members participating in cancer care at NTO program medical centers, including physicians, nurse practitioners, physicians' assistants and nurses.
Outcome Measures
Primary Outcome Measures
Number of raw telehealth visits
Fraction of patients engaging in at least one telehealth visit
Secondary Outcome Measures
Change in provider level Quality Oncology Practice Initiative (QOPI) score
Time of consultation to time of first appointment
Time of consultation to time of first treatment
Average total cost for cancer diagnosis, treatment and downstream HealthCare utilization
Timeline
Last Updated
November 4, 2024Start Date
August 19, 2024Today
May 12, 2025Completion Date ( Estimated )
January 1, 2027
Sponsors of this trial
Lead Sponsor
NYU Langone HealthCollaborating Sponsors
National Cancer Institute (NCI)