Actively Recruiting
Impact of Onco-sexology Support on the Quality of Life of Patients Newly Diagnosed for Cancer
Led by Hôpital Européen Marseille · Updated on 2025-07-01
168
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Onco-sexology as a supportive care for patients treated for cancer is still rarely discussed or even non-existent in 2022. However, it's recommended to integrate the preservation of sexual health throughout the treatment and post-cancer process, given the impact of cancer, treatments and the importance of intimate life for a majority of patients. Onco-sexology is one of the supportive care services validated by The French National Cancer Institute (INCa). It is also an objective of the 2014-2019 cancer plan and the 2017-2030 national sexual health strategy plan. Although sexuality is one of the fundamental needs of the human being, including in the case of a chronic disease or cancer diagnosis, the lack of training of health professionals to deal with intimate life, the difficulty to exchange on this subject between caregivers and patients, the lack of financial support for onco-sexology consultations, are all obstacles to the global management of oncology patients. However, it's a request from patients to be able to discuss the subject in an intimate way with a professional. While onco-sexology is already recommended as supportive care, a study on the impact of the delay in the management of sexual difficulties on quality of life could provide a sufficient level of evidence to change the practices and the care pathway of the oncology patient. Our objective is to study whether early management in onco-sexology has an impact on quality of life compared to late management (ie onco-sexology consultation before vs. after introduction of systemic oncological treatment).
CONDITIONS
Official Title
Impact of Onco-sexology Support on the Quality of Life of Patients Newly Diagnosed for Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 years
- Newly diagnosed with cancer, including patients receiving palliative care
- Able and willing to give free and informed written consent
You will not qualify if you...
- Pregnant or breastfeeding women
- Persons deprived of liberty by judicial or administrative decision
- Persons under legal protection measures or unable to express consent
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hôpital Européen Marseille
Marseille, France
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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