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Clinical Trials/NCT04758338
NCT04758338Active, not recruitingNot Applicable

Enhancing Cancer Care Of Rural Dwellers Through Telehealth and Engagement (ENCORE)

Debra Friedman10 sites in 1 country814 target enrollmentStarted: October 25, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
814
Locations
10
Primary Endpoint
Measure the effectiveness of a multi-level telehealth-based intervention

Study Overview

Brief Summary

Through a multi-level remote intervention, the Vanderbilt-Ingram Cancer Center (VICC) seeks to improve comprehensive cancer care delivery to patients residing in rural communities with persistent poverty. We plan to do this by using telehealth to broaden the reach of our NCI-designated comprehensive cancer center in these communities

Detailed Description

Objectives:

  • Evaluate the clinical effectiveness of a multi-level telehealth-based intervention for rural hospitals consisting of provider access to tumor board expertise that incorporates disease, patient and molecular tumor characteristics, together with patient access to a supportive care intervention to improve cancer care delivery.
  • Evaluate the facilitators and barriers to future larger-scale dissemination and implementation of the multi-level intervention, designed to enhance quality rural cancer care delivery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Provider and Patient:
  • At least 21 years of age or older and English speaking with the ability to provide informed consent
  • Oncology providers within designated VHAN oncology practices
  • Newly diagnosed or relapsed cancer patients of aforementioned oncology providers

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Measure the effectiveness of a multi-level telehealth-based intervention

Time Frame: Approximately 3 years

Estimate the facilitators to a future large-scale multi-level intervention

Time Frame: Approximately 3 years

Estimate the barriers to a future large-scale multi-level intervention

Time Frame: Approximately 3 years

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Debra Friedman
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Debra Friedman

Sponsor Investigator

Vanderbilt-Ingram Cancer Center

Study Sites (10)

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