This clinical trial evaluates the effectiveness of the Comprehensive Connected Cancer Care (C4) Program in helping patients with everyday needs related to their cancer care. The C4 Program is a multi-level program for cancer patients that leverages digital technology and combines psychosocial screening, patient navigation, remote patient monitoring, and education for patients and the healthcare team. This study may help researchers learn whether the C4 Program can advance health equity for underserved populations by improving timely access to community-focused, patient-centered, high-quality cancer care.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06326567.
Locations matching your search criteria
United States
Kentucky
Bowling Green
The Medical Center-Bowling GreenStatus: Active
Contact: Diego Cabrera
Hazard
Hazard Appalachian Regional Healthcare Regional Medical CenterStatus: Active
Contact: Samuel Dean Bailey
Lexington
University of Kentucky/Markey Cancer CenterStatus: Active
Contact: Timothy William Mullett
Phone: 859-257-5097
PRIMARY OBJECTIVES:
I. Assess effectiveness of the C4 Program on patient-level outcomes (verse [vs] usual care), including examining the impact on reducing disparities in patient-level outcomes.
II. Assess healthcare team-level outcomes of provider/staff education and intervention implementation.
III. Assess healthcare system-level outcomes of site-level performance on psychosocial screening outcomes and implementation process measures.
IV. Generate basic estimates of the costs and value of the C4 Program implementation from the perspective of hospital sites.
V. Assess the increase in the number of new community partnerships, broken down by organization type to identify which organizations address social determinants of health.
VI. Assess improvements in patient-level outcomes over the course of implementation.
OUTLINE: Participants are assigned to 1 of 2 Phases.
BASELINE PHASE: Patients receive usual care.
IMPLEMENTATION PHASE: Participants are assigned to 1 of 2 groups.
GROUP I: Patients participate in the C4 Program and complete five education modules over at least 10 minutes once a week (QW) for 4 months.
GROUP II: Healthcare team members participate in interviews on study.
Trial PhaseNo phase specified
Trial Typehealth services research
Lead OrganizationUniversity of Kentucky/Markey Cancer Center
Principal InvestigatorTimothy William Mullett
