Multidisciplinary assessment for supportive care in gynecological cancer patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to enhance supportive oncology care for patients recovering from gynecological cancers, specifically ovarian and endometrial cancers. Patients will be divided into three groups based on their supportive care needs, with those requiring support randomized into two groups: one receiving a personalized post-cancer plan with a multidisciplinary assessment in a day hospital, and the other receiving standard care without day hospitalization. The study will also include an observational cohort for patients with no supportive care needs. The main goal is to effectively identify and manage the supportive oncology care needs of patients in remission.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patient \> 18 years
* Patients in remission from first-line treatment of endometrial or ovarian/tumor/peritoneal cancer.
* Patient who has completed her initial treatment; patients on maintenance therapy are eligible.
* Fluency in French
* Patient with access to a telephone line
* Patient affiliated to a social security scheme
* Signature of informed consent prior to any specific study procedure

Exclusion Criteria:

* Any associated medical or psychiatric condition that could compromise the patient's ability to participate in the study
* Patient with locoregional or metastatic recurrence
* Patient deprived of liberty, under guardianship or curatorship
* Simultaneous participation in a therapeutic clinical trial

Where it's running

• CHU, Besançon
  Besançon, France Recruiting
• François Baclesse
  Caen, France Recruiting
• Centre Léon Bérard
  Lyon, France Recruiting
• Hopital Diaconesses Croix Saint-Simon
  Paris, France Recruiting
• Institut Curie, St Cloud
  Saint-Cloud, France Recruiting
• Chu
  Strasbourg, France Recruiting

Study contacts

• Study coordinator: Florence JOLY, Prof
• Email: f.joly@baclesse.unicancer.fr
• Phone: 02 31 45 50 50

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.