Clinical Trials Directory

Trials / Completed

CompletedNCT05577156

SexoMBC2 Non Interventional Study

Sexual Quality of Life and Metastatic Breast Cancer

Status
Completed
Phase
Study type
Observational
Enrollment
48 (actual)
Sponsor
Institut de Cancérologie de Lorraine · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study is composed of three paper self-questionnaires to be filled in by the patients included at distance (\> 6 months) from their diagnosis of metastatic breast cancer, in order to limit the impact of the announcement on the filling out the questionnaires. After verification of the eligibility criteria, the medical oncologist will present the study to patients coming to the ICL for a follow-up consultation as part of their regular care. The patients will meet with a clinical research nurse so that she can explain the again and answer any questions they may have. She will also give the patients the questionnaires questionnaires and will give a presentation of the questions asked. After this meeting, the patients will be given sufficient time to reflect on, which may extend until their next visit to the ICL, in order to express, if they wish, their opposition to participating in the study. If she agrees to participate, the patient can then complete the questionnaires as well as the complementary questionnaire and place them in a closed envelope to be given to the clinical research nurse. The completion of the questionnaires will be completely anonymous. The data of those who object to the use of their data will be deleted from the database. After the completion of the questionnaires, and in order to allow a benefit for the patient, a semi-directive interview in the form of a teleconsultation with a psycho-oncologist and sexologist will be offered. The interviews are not mandatory. The time to fill in the self-questionnaires is estimated at 30 minutes and the semi-directive interview can last up to one hour. Finally, at the end of the study, as part of her subsequent care, each patient participating in the study will have the possibility to renew a teleconsultation with the psycho-oncologist and sexologist if she feels the need. As the subject of the study may generate personal questions and lead to a request for psychological and/or sexological care.

Conditions

Interventions

TypeNameDescription
BEHAVIORALSelf-questionnaires and semi-structured interviewPatients will fill these questionnaires : BISF-W, QLQ-C30, QLQ-BR23 and if they agree answer to a semi-structured interview composed of 5 questions

Timeline

Start date
2022-12-05
Primary completion
2023-05-17
Completion
2023-05-17
First posted
2022-10-13
Last updated
2023-07-28

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05577156. Inclusion in this directory is not an endorsement.