RECRUITING

A Pilot Study of Genetic Testing Uptake Through Enhanced Oncology Nurse-Led Intervention

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Genetic factors are a significant determinant of the likelihood of developing various types of cancers. Identification of germline risk can have important implications for both patients and their families. Although estimates vary, pathogenic germline variants can be seen in \~3-17.5% of unselected patients with cancer with important clinical significance. Unfortunately, despite progress in multigene testing and the identification of heritable conditions, genetic counseling and testing (GCT) remains underutilized among cancer patients. Although there are multiple barriers to low testing, initial referral to GCT from the treating oncologist has been noted to be the most significant barrier. Nurse navigation has been shown to improve the timeliness of cancer care and patient outcomes across various cancer types and improve the uptake of genomic testing in cancer patients. Despite proven benefits, community cancer centers often face resource limitations that prevent them from consistently assigning a dedicated nurse navigator to cancer patients. However, community centers universally have oncology nurses who routinely educate patients about their systemic therapies. By enhancing the "therapy education" sessions, the investigators hypothesize that oncology nurses can bridge this gap and potentially identify eligible patients, provide essential education on the importance of genetic testing, and facilitate the referral process. The investigators propose a pilot randomized study to evaluate the potential effectiveness, acceptability, and feasibility of a novel, nurse-led "enhanced education" intervention specifically designed to increase the uptake of GCT in adult cancer patients.

Official Title

Genetic Testing Uptake Through an Enhanced Oncology Nurse-Led Intervention in Patients With Solid Tumors (GENESIS): A Pilot Study

Quick Facts

Study Start:2024-12-26
Study Completion:2025-09-26
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06436157

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults (≥ 18 years)
  2. * Diagnosed with a solid tumor cancer type that has established guidelines suggesting the utility of genetic testing in treatment (breast, ovarian, prostate, pancreatic, colon, Lynch syndrome-related cancers (colorectal, endometrial, gastric, ovarian, pancreatic, urothelial, brain (usually glioblastoma), biliary tract, small intestine), Li-Fraumeni syndrome tumor spectrum (e.g., soft tissue sarcoma, osteosarcoma, central nervous system tumors, breast cancer, adrenocortical carcinoma), etc.)
  3. * Eligible for GCT based on the current NCCN guidelines
  4. * Starting new systemic therapy or switching systemic therapy
  5. * Eligible for GCT as per the current NCCN guidelines
  6. * No prior genetic testing (or tested before 2014)
  1. * Prior GCT with test results available (if tested 2014 onwards)
  2. * Patients scheduled for treatment education with Advanced Practice Provider (typically reserved for more complex regimens)
  3. * Patients with cognitive impairments or severe psychological disorders that would limit their ability to understand the genetic counseling/testing information or give informed consent.
  4. * Any other condition that would, in the investigator's judgment, contraindicate the patient's participation in the clinical study due to safety concerns with clinical study procedures (e.g., patients requiring urgent therapy and/or inpatient chemotherapy initiation).
  5. * Patients who are currently participating in other clinical trials that could confound the outcomes of genetic testing uptake.
  6. * Prospective participants who, in the investigator's opinion, may not be able to comply with all study procedures (including compliance issues related to logistics).
  7. * Hematologic malignancy

Contacts and Locations

Study Contact

Rachel A Kitchen, CCRP
CONTACT
406-417-1576
rkitchen@ucdavis.edu

Principal Investigator

Ranjan Pathak, MD MHS
PRINCIPAL_INVESTIGATOR
Enloe Health

Study Locations (Sites)

Enloe Regional Cancer Center
Chico, California, 95926
United States
University of California, Davis
Sacramento, California, 95616
United States

Collaborators and Investigators

Sponsor: University of California, Davis

  • Ranjan Pathak, MD MHS, PRINCIPAL_INVESTIGATOR, Enloe Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12-26
Study Completion Date2025-09-26

Study Record Updates

Study Start Date2024-12-26
Study Completion Date2025-09-26

Terms related to this study

Keywords Provided by Researchers

  • Genetic Counseling and Testing
  • NCCN guidelines
  • Utilization
  • Feasibility
  • Nurse-led care coordination

Additional Relevant MeSH Terms

  • Solid Tumor, Adult