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Viewpoints on the Social Representations and Rationale Concerning the Choices of Patients, Doctors and Caregivers With Regard to the Management of Patients With Non-resectable Metastatic Cancer of the Colon, Stomach, Bile Ducts, Rectum, Pancreas or Lung, or Gastrointestinal Neuroendocrine Tumours (EOLE)

U

University Hospital Center (CHU) Dijon Bourgogne

Status

Terminated

Conditions

Non-resectable Metastatic Cancer of the Lung
Non-resecable Metastatic Cancer of the Pancreas
Non-resectable Metastatic Cancer of the Bile Duct
Non-resectable Metastatic Cancer of Gastrointestinal Neuroendocrine Tumour
Non-resectable Metastatic Cancer of the Rectum
Non-resectable Metastatic Cancer of the Rectosigmoid Junction
Non-resectable Metastatic Cancer of the Colon
Non-resectable Metastatic Cancer of the Stomach

Treatments

Other: Questionnaires
Other: Interviews

Study type

Observational

Funder types

Other

Identifiers

NCT03328065
LEJEUNE FdF 2016

Details and patient eligibility

About

Reflexion on the therapeutic strategies to implement in patients at the end of life is advancing rapidly in France. However, beyond the choices presented to patients, sometimes even the decision to carry on, to limit or to stop treatments is also questioned. This decision is subjective; it is influenced by the patient's representation system (emotions, beliefs, values, practices, etc). In addition, even though he or she is the focus of the decision, the patient is not alone; other actors, accompanying the patient, play an important role in the final decision making. These actors, namely the doctors and close relatives, are also influenced in their decision making. This coexistence of representation systems may interfere with objective indicators that help in decision making (functional, clinical and biological) or with the knowledge acquired by doctors in their training and may complicate the decision-making process.

Enrollment

36 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

I- PATIENTS

  • men or women
  • who have been informed about the study
  • and who have provided verbal consent to take part in the study
  • able to understand written and spoken French
  • with non-resectable metastatic cancer of: the colon, or the rectosigmoid junction or the stomach or bile ducts or rectum or gastrointestinal neuroendocrine tumor or lung (not small-cell cancer) or pancreas
  • with a caregiver designated as the principal caregiver (family, friend, neighbour)
  • who has consented to the principal caregiver taking part in a qualitative interview
  • able to take part in an interview lasting roughly one hour

II- CAREGIVERS

  • men or women
  • who have been informed about the study
  • who have provided verbal consent to take part in the study
  • able to understand written and spoken French
  • able to follow an interview lasting roughly one hour

III-DOCTORS

  • men or women
  • who have been informed about the study
  • who have provided verbal consent to take part in the study
  • specialised in specific organ or oncologist prescriber

Exclusion criteria

I- PATIENTS

  • under guardianship or ward of court
  • with a severe handicap (neurological disease: Parkinson, Alzheimer, other dementia, multiple sclerosis, severe mental retardation etc.)

II- CAREGIVERS

  • under guardianship or ward of court,
  • with a severe handicap (neurological disease: Parkinson, Alzheimer, other dementia, multiple sclerosis...),
  • with severe mental retardation impairing ability to understand.

Trial design

36 participants in 4 patient groups

Stable patients, early responders to treatment and caregivers
Treatment:
Other: Questionnaires
Other: Interviews
Stable patients and intermediate responders and c
Description:
Stable patients and intermediate responders to treatments and caregivers
Treatment:
Other: Questionnaires
Other: Interviews
Doctors
Treatment:
Other: Questionnaires
Other: Interviews
Patients in therapeutic escape and their caregivers
Treatment:
Other: Questionnaires
Other: Interviews

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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