RECRUITING

GC-PRO 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

The goal of the GC-PRO study is to try to make genetic counseling better for people of all backgrounds. We are asking participants to complete two surveys and to allow audio recording of their genetic counseling visit. The purpose of the study is to understand whether trying different ways of doing genetic counseling will lead to better experiences for patients. The research team is also working with partners from the Somali, Latino/Hispanic, Black/African American, and Hmong communities to make sure the research is being done in a way that will benefit underserved communities.

Official Title

GC-PRO Intervention

Quick Facts

Study Start:2025-01-03
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06671704

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. * Aged 18 years or older
  2. * individual OR their child has been referred to genetic counseling for family and/or personal history of hereditary cancer, cardiology condition, general genetics indication, or reproductive/prenatal indication at a participating study site
  3. * understand and be able to provide information for study forms and surveys in English.
  1. * Unable to provide informed consent
  2. * For pediatric genetic counseling referrals, individuals who are not the parent or legal guardian of the child will be excluded from participating.

Contacts and Locations

Study Contact

Elena Fisher
CONTACT
612-626-6743
fishe912@umn.edu

Principal Investigator

Heather Zierhut
PRINCIPAL_INVESTIGATOR
University of Minnesota

Study Locations (Sites)

University of Minnesota
Minneapolis, Minnesota, 55414
United States

Collaborators and Investigators

Sponsor: University of Minnesota

  • Heather Zierhut, PRINCIPAL_INVESTIGATOR, University of Minnesota

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 Date2025-01-03
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2025-01-03
Study Completion Date2026-06-30

Terms related to this study

Keywords Provided by Researchers

  • genetic counseling
  • cancer
  • heart disease
  • reproductive
  • prenatal
  • genetic

Additional Relevant MeSH Terms

  • Cancer
  • Cardiovascular Diseases
  • Prenatal Condition
  • Reproductive Condition
  • Genetic Condition