SexoMBC2 Non Interventional Study (SexoMBC2)
Sexual Quality of Life and Metastatic Breast Cancer
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Vandœuvre-lès-Nancy, France
- Institut de Cancerologie de Lorraine
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Major woman
- Patient with metastatic breast cancer, either initially or secondary metastatic breast cancer
- RH+/HER2- tumor
- Patient starting first line metastatic therapy or currently undergoing 1st line metastatic treatment
- Patient diagnosed with metastatic breast cancer 6 months or more
- WHO 1 or 2 patient
- Postmenopausal or not
- Patient able to understand the French language
Exclusion Criteria:
- Patient WHO>2
- Patient undergoing chemotherapy
- HER2+ or triple negative tumor
- Male
- Patient diagnosed with breast cancer less than 6 months ago
- Patient under guardianship, curatorship or safeguard of justice
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients
|
Patients will fill these questionnaires : BISF-W, QLQ-C30, QLQ-BR23 and if they agree answer to a semi-structured interview composed of 5 questions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of sexual quality of life in women with HR+/HER2- metastatic breast cancer in first-line treatment
Time Frame: Day 0
|
Patients will fill the questionnaire : BISF-W (Brief Index of Sexual Function for Women)
|
Day 0
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of overall quality of life in women with HR+/HER2- metastatic breast cancer in first-line treatment
Time Frame: Day 0
|
Patients will fill the QLQ-C30 questionnaire
|
Day 0
|
|
Assessment of overall quality of life in women with HR+/HER2- metastatic breast cancer in first-line treatment
Time Frame: Day 0
|
Patients will fill the QLQ+BR23 questionnaire
|
Day 0
|
|
Assessment of sexual and emotional intimacy
Time Frame: Day 0
|
semi-structured interview composed of 5 questions
|
Day 0
|
Collaborators and Investigators
Investigators
- Principal Investigator: VINCENT MASSARD, Institut de Cancerologie de Lorraine
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-A01192-41
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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