Image

Feasibility of an Advance Care Planning Intervention

Feasibility of an Advance Care Planning Intervention

Recruiting
18 years and older
All
Phase N/A

Powered by AI

Overview

Advanced Cancer patients hospitalized in a Cancer center inpatient unit have a dismal prognosis. Palliative Care interventions have shown multiple benefit for those patients, regarding quality of life, symptom management, illness understanding and aggressiveness of care criteria. Although Advance Care planning (ACP) is part of usual Palliative Care, specific interventions dedicated to ACP are understudied.

This study aims at showing that a simple and systematic Advance Care Planning intervention is likely to clarify the understanding of the goals of care by patients, to help with ACP documentation and and potentially to modify the trajectory of illness for patients during and after hospitalization.

Description

PREVOIR is a randomized, single-center, two-arm trial: patients from experimental arm will benefit from a systematic interview on the care plan whereas patients from control arm will received standard cares.

Eligibility

Inclusion Criteria:

  • Patients aged 18 years or older
  • Patients with a diagnosis of advanced or metastatic solid cancer
  • Patients hospitalized in a conventional oncology, radiotherapy or hematology department
  • Agreement obtained from the referring oncologist or senior doctor responsible for the patient during hospitalization
  • Patient hospitalized for less than 7 days
  • Patients who have not yet written advance directives
  • Signature of informed consent

Exclusion Criteria:

  • Patients treated for hematologic malignancies
  • Presence of uncontrolled symptoms that do not allow an interview to be carried out
  • Patients with planned hospitalization for chemotherapy or biopsy or performance of a procedure
  • Patients < 18 years old or patients ≥ 18 years old under supervision
  • Patients placed under judicial protection or guardianship
  • Decompensated neuropsychiatric disorders
  • Comprehension problems
  • Patients without social security
  • Allophone patients

Study details
    Neoplasms

NCT06149312

Institut de cancérologie Strasbourg Europe

20 March 2024

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.