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Implementing VTE Prevention in Ambulatory Cancer Care

Implementing VTE Prevention in Ambulatory Cancer Care

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07292376
Enrollment
25
Registered
2025-12-18
Start date
2025-10-01
Completion date
2026-07-30
Last updated
2025-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasms, Venous Thromboembolism

Brief summary

assess effectiveness of a , compared with usual care, to assess The goal of this study is to learn if a modified clinical program can improve adherence to guideline recommendations for prevention of venous thromboembolism in ambulatory patients with cancer. The main question\[s\] it aims to answer are: Does the modified program improve number of ambulatory oncology patients starting systemic treatment getting VTE risk-assessment? Does the modified program improve the number of patients receiving appropriate preventative anticoagulation? Researchers will compare to usual care (no clinical program). Participant clinicians will be asked to * receive education about VTE prevention recommendations * carry out risk assessment, anticoagulation discussions, and document the results Participant patients will receive care from clinicians participating in the study as part of their cancer care.

Interventions

OTHERClinical program

Revised Vermont Model clinical program, including standardized education and training for oncology care team, clinical decision support and revised workflow for VTE risk assessment and thromboprophylaxis.

Sponsors

University of Vermont
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinicians: practicing oncologist at study clinic site (UVMMC) * Patients: diagnosis of cancer; starting new systemic cancer-directed therapy at a study clinic site under the direction of the enrolled clinician

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Documented VTE risk assessment30 days after new patient appointmentProportion of new patients who have documented VTE risk assessment

Secondary

MeasureTime frameDescription
Appropriate thromboprophylaxis30 days after new patient appointmentProportion of identified high-risk patients with prescription for thromboprophylaxis and low-risk patients without thromboprophylaxis

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026