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OpenTrials
Active, Not Recruiting

NCT Number: NCT05731661

Optimize the Support of Patients in Pelvic Onco-gynecology Through Adapted Support Care in the Post-cancer Period. AFTERGYN Pilot Phase

While the sequelae and toxicities after ovarian and endometrial cancer treatments are well described in the literature, the actual needs of patients for supportive oncology care remain poorly documented. Moreover, there is no data available to estimate the complexity of the oncological support care actions to be implemented.

It is expected that an evaluation of the needs for supportive oncology care and its organization in day hospitalization for supportive oncology care will lead to an improvement in personalized post-cancer follow-up for these patients and to an improvement in their long-term quality of life.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Centre Francois Baclesse

Caen, 14076, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient > 18 years old
  • Patient in complete remission after first-line treatment for endometrial or ovarian/fallopian tube/peritoneal cancer
  • Patient having completed her initial treatment; patients with maintenance treatments are eligible
  • Mastery of the French language
  • Patient with a telephone line
  • Patient affiliated to a social security scheme
  • Signature of informed consent before any specific procedure related to the study

Exclusion criteria

  • Any associated medical or psychiatric conditions 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

Treatment and study plan

Day hospitalization in support care with meeting with support care professionals and coordination of actions by the advanced practice nurse

Other

During this day hospitalization, patients will meet with different specialized professionals depending on the support care needs identified.

Delivery of useful information according to support care needs, concerning support care professionals in the city

Other

Delivery of useful information according to support care needs, concerning support care professionals in the city

Delivery of a personalized post-cancer plan

Other

Delivery of a personalized post-cancer plan

Primary outcomes

  1. Proportion of patients who used at least one of the oncology support services recommended in the Personalized After-Cancer Care Plan within 4 months of receiving the Personalized After-Cancer Care Plan

    Time frame: Up to 4 months

Secondary outcomes

  1. Proportion of patients with sequelae after the initial treatment of their cancer, as well as the type and grade of the sequelae, based on the National Cancer Institute's screening grids (levels 1 and 2) during the consultation with a nurse referent

    Time frame: Up to 4 months

  2. Description of the types of oncological support care needs identified

    Time frame: Up to 4 months

  3. Proportion of patients with identified cancer care needs (at least one cancer care need to be implemented) 4 months after the submission of the Personalized Cancer Care Plan

    Time frame: Up to 4 months

Sponsors and collaborators

Lead sponsor

Centre Francois Baclesse

Other

Collaborators

  • Ligue contre le cancer, France

Registry information

Acronym: AFTERGYN

Important dates

Study start
2023
Primary completion
2025
Study completion
2027
First posted
Feb 16, 2023
Registry last updated
Jan 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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