Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06550687

Study of Cancer Patients' Preferences for Genetic Information Modalities Preceding Theranostic Exome Analysis.

Led by Centre Georges Francois Leclerc · Updated on 2025-02-18

80

Participants Needed

2

Research Sites

110 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Currently, the EXOMA2 study (NCT04614480) offers earlier and more comprehensive exome analysis in the management of cancer patients than EXOMA. Based on the active EXOMA2 patient file, the INFOGene study offers the opportunity to study patient-physician communication, to assess patient preferences with regard to different information modalities concerning theranostic exome analysis, and to reflect on information modalities to ensure optimal patient comprehension of the information provided. The qualitative cross-sectional study includes a dual observational and interventional component involving cancer patients. The patients will come from the EXOMA 2 active file at Dijon University Hospital and the CGFL.

CONDITIONS

Official Title

Study of Cancer Patients' Preferences for Genetic Information Modalities Preceding Theranostic Exome Analysis.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient identified for inclusion in the EXOMA 2 study (exome analysis request)
  • Available to receive different types of information
  • Fluent in French
  • No prior oncogenetic consultation
  • Informed of the study objectives and given written non-objection to participate
  • Authorizes audio recording of consultations and interviews
Not Eligible

You will not qualify if you...

  • Patient who refused to participate in the EXOMA2 study (for phase 3 patients only)
  • Has a psychiatric, cognitive or neurological disorder that makes participation impossible
  • Working in the field of genetics

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Centre Georges-François Leclerc

Dijon, France, 21000

Actively Recruiting

2

CHU François Mitterand

Dijon, France, 21000

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

OTHER

Number of Arms

3

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