eHealth Delivery Alternative for Cancer Genetic Testing for Hereditary Cancer

NCT05427240 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2026-01-16

No results posted yet for this study

Summary

This randomized non-inferiority study will use a 2x2 design where traditional standard-of-care pre-test (visit 1) and post-test (visit 2: disclosure) counseling delivered by a genetic counselor are replaced with a self-directed web-based eHealth intervention to provide critical data to inform optimal ways to deliver clinical genetic testing in eligible individuals, while maintaining quality of care and favorable cognitive, affective and behavioral outcomes.

Conditions

Interventions

OTHER

Pre-Test Intervention

Secure and accessible by private code only, the web-based intervention will provide users with a the results of their clinical genetic testing results and a detailed summary of what those results mean. Additionally, an individualized summary will also be included.

OTHER

Standard of Care

Standard of Care with a Genetic Counselor by Remote Services

OTHER

Post-Test Intervention

Secure and accessible by private code only, the web-based intervention will provide users with a the results of their clinical genetic testing results and a detailed summary of what those results mean. Additionally, an individualized summary will also be included.

Sponsors & Collaborators

  • Fox Chase Cancer Center

    collaborator OTHER
  • National Cancer Institute (NCI)

    collaborator NIH
  • Abramson Cancer Center at Penn Medicine

    lead OTHER

Principal Investigators

  • Angela R Bradbury, MD · University of Pennsylvania

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-28
Primary Completion
2025-12-24
Completion
2026-07-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05427240 on ClinicalTrials.gov