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Rapid First Contact Using Virtual Visits to Improve Time-To-Treatment for Uterine Cancer

Not Applicable
Withdrawn
Conditions
Uterine Cancer
Interventions
Behavioral: Virtual visit
Behavioral: Office visit
Registration Number
NCT03583736
Lead Sponsor
Case Comprehensive Cancer Center
Brief Summary

This project aims to evaluate whether rapid first contact with the oncologist the same day or the next day after pathologic diagnosis contributes to a decreased time to treatment, decreased patient anxiety and increased patient satisfaction.

Detailed Description

Time to treatment (time from disease diagnosis to initiation of treatment) impacts outcomes in uterine cancer. When controlled for stage, patients with longer time to treatment tend to have less favorable outcomes. Similarly, longer time to treatment has a negative impact on patients' quality of life and markers for anxiety. Our experience at this institution suggests that the time to referral (time from uterine cancer diagnosis and the patients' first encounter with the oncologist) is variable and presents the greatest opportunity for decreasing time to treatment. Among the factors that contribute to the time to referral are the time taken by the referring provider to relay the diagnosis to the patient, time taken to schedule an appointment with the specialist, and the patient's availability to keep an appointment.

Virtual visits provide an opportunity to expedite consultation with the treating oncologist by removing some of the barriers that delay face-to-face visits. Among these barriers are patients' availability for a short notice face-to-face visit based on their work or family obligations, access to transportation, and mental preparedness.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria
  • Uterine cancer diagnosis on biopsy read by Cleveland Clinic Pathology Department
  • Patients must be willing to participate in a virtual visit as the initial meeting with an oncologist at the Cleveland Clinic.
  • Receive care at Fairview Hospital, Hillcrest Hospital or Cleveland Clinic Main Campus
  • Internet connected smartphone or internet connected computer with webcam
  • Participants must have email access
  • English speaking
  • Competent to make clinic decisions
Exclusion Criteria
  • No diagnosis of uterine cancer

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Rapid first contact virtual visitVirtual visitSubjects will accept the offer of a virtual visit after being contacted by the nurse to offer a virtual visit with the oncologist prior to the in person office visit once a diagnosis has been confirmed. Subjects will be randomized after accepting offer of a virtual visit.
First contact in person office visitOffice visitSubjects will accept the offer of a virtual visit after being contacted by the nurse to offer a virtual visit with the oncologist prior to the in person office visit once a diagnosis has been confirmed. Subjects will be randomized after accepting offer of a virtual visit.
Primary Outcome Measures
NameTimeMethod
Time to treatment following diagnosis to treatment initiation30 days

How long between diagnosis to treatment

Secondary Outcome Measures
NameTimeMethod
Number of patients with improved satisfaction scores30 days

Determine whether the addition of a rapid virtual visit improves patients satisfaction

Number of patients willing to pay for a virtual visit30 days

Assess patients valuation of virtual visits by measuring their willingness to pay

Amount of anxiety demonstrated when virtual visits are added30 days

Level of anxiety using GAD-7

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