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NCT05406024Completed

Feasibility Study CORPPS

FEASIBILITY STUDY on the Use of a DIGITAL PLATFORM for Physical and Psychosocial RECONDITION After Major Neoplastic Surgery

Source: ClinicalTrials.gov · Last updated 11 Dec 2025

Brief summary (registry, in English)

The incidence of cancer in France has increased by +135% to reach nearly 400,000 new cases in 2018. The ten-year cancer control strategy 2021-2030 and the health innovation plan have defined strategic axes. Almost all of these axes are addressed in our project. Firstly, the main objective of our study is to improve the quality of life of patients. Secondly, pharyngolaryngeal and oesophageal cancers are among the cancers with a poor prognosis in adults. Thirdly, the project provides access to personalised supportive care for all patients at all times. Finally, the secondary objectives of this study are the prevention of post-operative complications (infectious, thrombo-embolic, pain...).

Status (registry)
Completed
Study type
Observational
Enrollment
30 (actual)
First submitted
24 May 2022
Start date
3 Apr 2023
Primary completion date
19 Apr 2024
Lead sponsor
University Hospital, Lille
NCT number
NCT05406024

What you commit to

  • Study type: Observational
  • Participants enrolled: 30
  • From 3 Apr 2023 to the primary completion date, 19 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient who did not follow the previously described course of care prior to admission to the ward

Other

  • Esophagectomy with total circular pharyngo-laryngectomy
  • Total esogastrectomy
  • Illiterate, visually impaired patient
  • Minor, or adult under guardianship or curatorship, under judicial protection, person deprived of liberty

Who the study is looking for

  • Hospitalized for initial surgical management of esophageal or laryngeal cancer
  • Admitted to a conventional ward after partial oesophagectomy or total laryngectomy in a neoplastic setting
  • Patient giving consent to participate in the study
  • Affiliated to the compulsory health insurance scheme, regardless of the scheme

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Universtaire
Coordinator of this site? Confirm its status
LilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.