Trials / Recruiting
RecruitingNCT06553612
Impact of a Multidisciplinary Assessment in Day Hospitalization Versus Standard Care on the Deployment of Supportive Oncology Care Recommended by the Personalized Post-cancer Plan in Patients at the End of Initial Treatment for Gynecological Ovarian and Endometrial Cancer Endometrial Cancer
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 268 (estimated)
- Sponsor
- Centre Francois Baclesse · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This project proposes a structuring of supportive oncology care for the recovery phase after gynecological cancer (ovarian/trope/peritoneum or endometrium). Patients will be divided into three groups based on the identification of oncological support care needs. Patients with supportive oncology care needs will be randomized into two groups: the experimental group, receiving a personalized post-cancer plan with a multidisciplinary assessment of supportive oncology care needs in a day hospital and coordinated follow-up by the referring study nurse, and the control group, receiving a personalized post-cancer plan without a day hospital. Randomization will be stratified according to tumor location (ovary vs. endometrium), use of supportive oncology care during treatment, and treatment center. Patients with no need for supportive oncology care will be followed in an observational cohort. The main objective is to identify and manage the supportive oncology care needs of patients in remission from endometrial or ovarian cancer to improve their quality of life and post-treatment follow-up. A medico-economic analysis will be performed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Multidisciplinary assessment | Delivery of a personalized post-cancer plan with multidisciplinary assessment of oncology support care needs in a day hospital |
| OTHER | Standard assesment | Delivery of a personalized post-cancer plan without a day hospital |
| OTHER | Observational cohort | Patients with no cancer sequelae, no adverse effects and no need for oncological support care will not be randomized, but will be followed as part of an observational cohort |
Timeline
- Start date
- 2024-06-07
- Primary completion
- 2027-09-07
- Completion
- 2028-06-07
- First posted
- 2024-08-14
- Last updated
- 2026-01-08
Locations
13 sites across 1 country: France
Source: ClinicalTrials.gov record NCT06553612. Inclusion in this directory is not an endorsement.