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Support Pathway for ENT Cancer Patients in a Support Care Day Hospital (PAKO-HDJ)

C

Clinique Pasteur Lanroze

Status

Enrolling

Conditions

Otorhinolaryngologic Neoplasms

Treatments

Procedure: Consultations with paramedics

Study type

Interventional

Funder types

Other

Identifiers

NCT06512662
2023-18-CPL

Details and patient eligibility

About

Cancers of the upper respiratory / digestive tract are a major public health problem, ranking 5th among the most common cancers. Surgery plays a central role in the recommended treatments for this type of pathology. The surgical procedure and its after-effects can be anxiety-provoking and have a major psychological, physical and social impact on patients over the long term.

Our institution's standard protocol is based on a pre-operative supportive care day hospital. The aim of this study is to compare our current care pathway with a more extensive interdisciplinary care pathway focused on patients' needs, in order to reduce anxiety and improve the quality of life of patients undergoing surgery for cancers of the upper respiratory / digestive tract.

Our aim is to use a prospective single-centre interventional study to assess the impact of adding three post-operative day hospitals to the existing care pathway in terms of reducing anxiety and improving the quality of life of patients undergoing surgery.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patient undergoing surgery for VADS cancer requiring at least one night's post-operative hospitalisation
  • Understanding of spoken and written French
  • Patient covered by a social security scheme

Exclusion criteria

  • Protected patient under a protective measure or legal safeguard
  • Pregnant or breast-feeding patients
  • Patients suffering from major cognitive disorders
  • Patients with major anxiety disorders prior to the onset of cancer

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Control
No Intervention group
Supportive care
Experimental group
Treatment:
Procedure: Consultations with paramedics

Trial contacts and locations

1

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Central trial contact

Camille Vuarin, APN

Data sourced from clinicaltrials.gov

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