Onco-primary Care Networking to Support TEAM-based Care

NAActive, not recruitingINTERVENTIONAL
Enrollment

313

Participants

Timeline

Start Date

June 14, 2021

Primary Completion Date

June 30, 2026

Study Completion Date

June 30, 2026

Conditions
Blood PressureHypertensionCancerCancer, BreastCancer of ProstateCancer ColorectalCancer, EndometrialCancer of Head and NeckNon Small Cell Lung CancerCVD - Cardiovascular DiseaseDiabetes MellitusHypercholesterolemiaDiabetesCancer of EsophagusCancer of LiverCancer, Renal CellCancer of PancreasCancer Ovaries
Interventions
BEHAVIORAL

iGuide Intervention (Self-guided)

The iGuide Intervention consists of two patient-level and four PCP-level components. These components include: (1) the patient-level brief video vignettes with a written summary; and (2) patient-facing webinars. The investigators will not use any institutional branding in the videos, printed materials, or recorded webinars so that these deliverables can be used in other settings.

BEHAVIORAL

iGuide 2 Intervention (Tailored/Targeted)

"The iGuide2 patient-level intervention will use a stage-based, tailored approach to four monthly 5-minute video vignettes that incorporates a pre-video worksheet. The investigators will send the worksheets and video vignettes in the method preferred by the patient.~The targeted iGuide 2 PCP-level intervention will include a cancer specialist-facing dashboard that includes the specialists's patients who are enrolled in the study and are in the intervention arm. The HEDIS quality measures for our three CVD comorbidities will be used. The dashboard will be populated with data available in Epic for the specific patient. If some information is missing (i.e., there is no lipid profile in the laboratory tab), the dashboard will query the PCP via an e-consult, asking to supply the information. Bimonthly, starting with the second randomization, an asynchronous specialist-to-PCP e-consult will be sent to PCPs whose patient(s) do not meet all three of the HEDIS quality metrics."

BEHAVIORAL

Control

Participants randomized to the control group (n=400) will receive current guideline-concordant cancer care. The investigators will also provide information for healthy living during and after cancer and for preparing for transition from cancer therapy to follow-up care. Monthly, patient education material on healthy living will be sent to the participants via the patient portal or by mail, based on participant preference. At the completion of therapy, they will be provided the NCI Facing Forward:Life After Cancer booklet. Note, this approach is not fully equivalent to an attention control as there will be touch points in the iGuide and iGuide2 interventions that the investigators cannot match for the control group. Also, the research team will not engage the PCPs in clinics randomized to the control group.

Trial Locations (1)

27710

Duke University Medical Center, Durham

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Duke University

OTHER