Effectiveness of Central Oncology Navigation and the Use of an ORN

Launched by UNC LINEBERGER COMPREHENSIVE CANCER CENTER · Sep 25, 2024

Keywords

ClinConnect Summary

This clinical trial is looking at how well a new support system for cancer patients works. It compares two approaches: the first is called "central oncology navigation," which helps guide patients through their cancer care, and the second adds a special role called an "oncology research navigator" (ORN) to this system. The trial includes two groups of patients: one group with newly diagnosed genitourinary or thoracic cancers, who will receive the navigation support for the first time, and another group with gastrointestinal, hematology, or breast cancers, who may receive the extra help from the ORN in addition to their standard care.

To participate in this study, you need to be at least 18 years old, have a confirmed cancer diagnosis, and have a new patient appointment at a UNC Medical Center. You will need to give your consent to take part in the study. If you join, you can expect to receive support for your cancer care and potentially be connected to helpful services and clinical trials over a three-month period. The study aims to see how these support roles impact your quality of life and overall experience with cancer treatment.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • In order to participate in this study a subject must meet all of the eligibility criteria outlined below.
• • Informed consent obtained to participate in the study and HIPAA authorization for release of personal health information.
• • Subject is willing and able to comply with study activities based on the judgement of the investigator.
• • Age ≥ 18 years at the time of consent.
• • Subject has a new patient appointment for cancer care at a UNC Medical Center and a confirmed cancer diagnosis.
• Exclusion Criteria:
• • Lack of internet access.
• • Inability to understand the English language.
• • Psychological or other disability resulting in the inability to provide informed consent.