Trial to Compare eConsent With Standard Consent Among Prospective Biobank Participants

Completed · Not applicable

Conditions studied: Lynch Syndrome

In brief

The goal of this trial is to determine whether the Sage eConsent framework (presented using an electronic application) is non-inferior to traditional, paper-based, human-mediated consent-and therefore could be part of an acceptable population screening approach to identifying patients and others with actionable hereditary syndromes-and to increase basic knowledge about patients' informational needs about different aspects of genetic/omic screening. After receiving either 1) the traditional consenting approach, or 2) a consenting approach presented on an electronic tablet, the investigators will test for differences between these two arms in a variety of outcome measures including objective and perceived comprehension, time spent and informational needs, and enrollment decision, among others.

Key facts

Study ID
NCT04131062
Run by
Geisinger Clinic
People needed
703
Starts
2019-11-01
Expected to finish
2022-05-19
Last updated by the study team
2022-12-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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