RECRUITING

Caris Biorepository Research Protocol

Conditions

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

The Biorepository for Caris Life Sciences is designed for the purpose of making quality biospecimens and associated clinical data available for research studies related to advancing precision medicine and improving care for patients. The Caris Biorepository is a repository of prospectively collected biological specimens and associated clinical and demographic data gathered from multiple sources to be stored, used and shared for research. Caris Life Sciences will maintain the data and specimens and will control access to and use of the information and specimens by multiple individuals for multiple purposes which may evolve over time.

Official Title

The Caris Biorepository Research Protocol

Quick Facts

Study Start:2010-11
Study Completion:2025-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT01499394

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 years of age or older
  2. * Capacity to provide informed consent
  1. * Due to the complexity of state and federal requirements governing the participation of prisoners in research, prisoners-patients will not be approached for participation in the Caris Biorepository.
  2. * Minor subjects will not be included in the Caris Biorepository, as it is possible biospecimens and data may be stored beyond the time limitations of assent and it may be impracticable to re-consent these subjects once they become adults.
  3. * Individuals who lack the capacity to give informed consent

Contacts and Locations

Study Contact

Mary Baker
CONTACT
carisresearch@carisls.com

Principal Investigator

Zoran Gatalica, MD, DSc
PRINCIPAL_INVESTIGATOR
Caris Life Sciences

Study Locations (Sites)

Phoebe Putney Memorial Hospital
Albany, Georgia, 31701
United States
The Iowa Clinic, PC
West Des Moines, Iowa, 50266
United States
Eastern Carolina Women's Center
New Bern, North Carolina, 28562
United States
Advantage Clinical Research
Nashville, Tennessee, 37203
United States
Overlake Hospital
Bellevue, Washington, 98004
United States
Walla Walla Clinic
Walla Walla, Washington, 99362
United States
CAMC Clinical Trials
Charleston, West Virginia, 25304
United States

Collaborators and Investigators

Sponsor: Caris Science, Inc.

  • Zoran Gatalica, MD, DSc, PRINCIPAL_INVESTIGATOR, Caris Life Sciences

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 Date2010-11
Study Completion Date2025-11

Study Record Updates

Study Start Date2010-11
Study Completion Date2025-11

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer