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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Georges Francois Leclerc

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Sequential

Treatments tested in this trial

  • Cancer patients' preferences regarding genetic information modalities prior to theranostic exome analysis

    Other intervention

    Phase 1: Observation of doctor-patient consultations Phase 2: Adaptation of information tools Phase 3: Assessment of understanding of information tools

Treatment groups

80 Participants
are divided into 3 treatment groups
Group A: Phase 1:Observe communication between physicians and cancer patientsOther 1 intervention
Group B: Phase 2 : Revisit existing information media (GGC information note and video).No intervention 0 interventions
Group C: Phase 3:Assess patients' preferences with regard to 3 information modalitiesOther 1 intervention

Trial outcomes

Primary outcomes

1

Concepts of communication and preferences.

The various interviews (phases 1 and 3) will provide an insight into patients' level of health literacy, which may explain the ease or difficulty of exchanges with the doctor (phase 1), as well as patients' preferences for one type of information over another (phase 3).

Time frame
Through study completion, an average of 21 months.

Secondary outcomes

Other outcomes

Sponsors and contacts

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