RecruitingNot ApplicableNCT06583460

Systematic Intervention to Improve Sexual Dysfunction

Systematic Intervention to Improve Sexual Dysfunction in Adjuvant Breast Cancer Patients

Sponsor

Center Eugene Marquis

Enrollment

60 participants

Start Date

Dec 9, 2024

Study Type

INTERVENTIONAL

Conditions

Breast Cancer Female Localized Cancer

Summary

The aim of this clinical trial is to compare the benefit of early, systematic, multidisciplinary oncosexological care versus on-demand care on the sexual health of women with breast cancer.

Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study addresses sexual dysfunction in women who have been treated for early-stage breast cancer. Cancer treatments like surgery, chemotherapy, hormone therapy, and radiation can significantly affect sexual health and intimacy. This trial tests a structured intervention program to help women identify and manage these issues. **You may be eligible if...** - You are a woman aged 18 or older (menopausal or not) - You have been diagnosed with localized breast cancer (with or without lymph node involvement) - Your initial treatment was surgical removal of the tumor, with any combination of additional therapies - You are affiliated with a participating healthcare system **You may NOT be eligible if...** - You have metastatic (stage IV) breast cancer - You have a pre-existing condition that significantly affects sexual health unrelated to your cancer treatment - You are unable to participate in the intervention program Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHEREarly and systematic oncosexological supporting care

Each patient included in the study will be cared by an anthropologist and a sexologist. This therapeutic support care will be based on : * 2 qualitative semi-directive interviews (Baseline and M18), * 2 individual consultations with questionnaires (Baseline and M18). The qualitative semi-structured interviews will be conducted with the anthropologist, and the individual consultations with the sexologist. At the end of the first oncosexology consultation, patients will be given the opportunity to decide whether or not to accept further systematic oncosexology support care, which will be based on : * 3 individual and/or couple consultations, * 3 group workshops. Patients are under no obligation to accept this additional oncosexology support care.