eHealth Delivery Alternative for Cancer Genetic Testing for Hereditary Cancer
Recruiting now · Not applicable
Conditions studied: Cancer
In brief
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.
Key facts
- Study ID
- NCT05427240
- Run by
- Abramson Cancer Center at Penn Medicine
- People needed
- 1000
- Starts
- 2022-09-28
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2026-01-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- 18 years of age or older
- Speak and understand English
- Male or Female
- No prior germline genetic testing
- Meet current National Comprehensive Cancer Network (NCCN) guidelines for germline genetic testing
You may not qualify if…
- Communication difficulties such as:
- Uncorrected or uncompensated hearing and/or vision impairment
- Uncorrected or uncompensated speech defects
- Uncontrolled psychiatric/mental condition or severe physical, neurological or cognitive deficits rendering individual unable to understand study goals and tasks
Where it is running
- Abramson Cancer Center at the University of Pennsylvania — Philadelphia, Pennsylvania, United States (enrolling)
Full record on ClinicalTrials.gov
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