RECRUITING

Universal Germline Testing in the Community

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

This study seeks to enroll participants who have a diagnosis of a solid tumor cancer and are willing to undergo germline genetic testing for cancer risk. At baseline, patients will be asked to provide 2 types of blood samples: 1 tube for clinical genetic testing and 2 tubes for future research use. A tumor sample from a previous resection or biopsy will also be obtained and sent to the sponsor. The clinician will be asked to provide relevant medical history and demographic information to the sponsor in the form of electronic case report forms.

Official Title

Prospective Community Cancer Clinics-based Approach to Optimize Germline Testing in Cancer Patients in Rural Setting to Address Racial Disparities: UNIversal Germline Testing in the communitY (UNITY) Study

Quick Facts

Study Start:2022-06-01
Study Completion:2025-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05416710

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. * Patient has consented to germline genetic testing
  2. * Patient has a histologically confirmed diagnosis of a solid tumor cancer
  3. * Patient is willing to release previously collected tissue sample
  4. * Patient is willing to provide research blood samples
  5. * Patient must be at least 18 years of age
  1. * Patient is unable to consent.
  2. * Patient with hematologic malignancy

Contacts and Locations

Study Contact

Lee Ifhar
CONTACT
5512150508
lee.ifhar@invitae.com
Brandie Leach
CONTACT
brandie.leach@invitae.com

Study Locations (Sites)

Carolina Blood and Cancer Care Associates, PA'
Rock Hill, South Carolina, 29732
United States

Collaborators and Investigators

Sponsor: Invitae Corporation

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 Date2022-06-01
Study Completion Date2025-06-01

Study Record Updates

Study Start Date2022-06-01
Study Completion Date2025-06-01

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer
  • Solid Tumor
  • Solid Tumor, Adult