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CancerPALPHA-1NCT04717440

Assessment of the Reasons for Accepting or Refusing Early Palliative Care

An observational study of Cancer, run by Centre Leon Berard at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This is a prospective, multicentre study, considered as " non-RIPH ("Recherche n'Impliquant pas la Personne Humaine - Research that does not involve humans ". Indeed, the patient's participation in the study and the completion of the various questionnaires has no impact on patient's safety and is not likely to change… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cancer
How many people
37 participants
Where
1 siteFrance
Study dates
4 Feb 2021to 22 Mar 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: This is a prospective, multicentre study, considered as " non-RIPH (Recherche n'Impliquant pas la Personne Humaine - Research that does not involve humans ". Indeed, the patient's participation in the study and the completion of the various questionnaires has no impact on patient's safety and is not likely to change patient's management. Patients accepting to take part to an early phase trial will be proposed to participate in the PALPHA-1 trial. They can accept or refuse to have palliative supportive care. Patients' follow up will be performed according to the palliative standard procedures.

Who may be able to join

  • Age over 18
  • Patient included in an early phase clinical trial
  • Patient who has not been taken in charge for palliative care
  • Life expectancy of at least 16 weeks
  • Patient not opposed to data's collection and processing for the study
  • Patient affiliated to a social security system

Who cannot join

  • Patient unable to read/understand the French language
  • Patient with psychological disability (e.g. too great vulnerability, psychiatric disorder) or physical disability (e.g. physical / motor disability)
  • Patients under autorship, curators or legal protection,
  • Patients already participating in a clinical trial or interventional study related to supportive care.

Trial locations and contacts

1 site in 1 country.

France1 site
  • Centre Leon Berard

    Lyon, 69008

Other trials in France

About this study

Official title: Assessment of the Reasons for Accepting or Refusing Early Palliative Care by the Patients Included in an Early Phase Clinical Trial

This is a prospective, multicentre study, considered as " non-RIPH ("Recherche n'Impliquant pas la Personne Humaine - Research that does not involve humans ". Indeed, the patient's participation in the study and the completion of the various questionnaires has no impact on patient's safety and is not likely to change patients' management. Patients accepting to take part to an early phase trial will be proposed to participate in the PALPHA-1 trial. They can accept or refuse to have palliative supportive care.

The main objective of this study is to assess the reasons for accepting and refusing early palliative care in patients included in an early phase clinical trial. The secondary objectives will enable to describe and analyze the number (effective) and the rate (%) of acceptance and/or refusal of early palliative support, to assess patients' understanding and perception of the " combined " management by comparing the semantic content of the patient-investigator ecological interaction during the proposal for inclusion in the trial (i.e. what was explicitly said), with that of the semi-structured post-consultation inclusion interviews ( ie what the patients understood, perceived), to compare the quality of life and the anxiety-depression of patients according to their acceptance or refusal of the mixed care at the inclusion and at the end of the early phase trial, to compare the clinical, medical and socio-demographic characteristics of the patients, the overall survival of patients according to their acceptance or refusal of the combined management and finally for the patients accepting the Palliative Care Management (PCM), to describe throughout the study, the patients' compliance to palliative supportive care undertaken.

Read the detailed description

In a context of promotion of precision medicine, if palliative management and inclusion in an Early Clinical trial Phase (ECP) may at first glance appear antagonistic, some authors support the idea of a possible synergy in order to improve quality of life, reduce symptoms of exhaustion linked to treatment side effects and allow patients to complete their treatment protocol. To date and to our knowledge, few studies have assessed the brakes and/or levers for patient acceptance and/or refusal as well as the feasibility of a such mixed therapeutic management therapeutic. In this context, the beliefs and representations of patients must be taken into account in the decision-making process, which is also governed by the social norms of the caregiver-patient relationship. A better understanding of patients' acceptance and/or refusal of palliative care is an essential and innovative prerequisite for better understanding the processes involved at this stage of the care process.

The main objective of this study is to assess the reasons for accepting and refusing early palliative care in patients included in an early phase clinical trial. The secondary objectives will enable to describe and analyze the number (effective) and the rate (%) of acceptance and/or refusal of early palliative support, to assess patients' understanding and perception of the " mixed " management by comparing the semantic content of the patient-investigator ecological interaction during the proposal for inclusion in the trial (i.e. what was explicitly said), with that of the semi-structured post-consultation inclusion interviews ( ie what the patients understood, perceived), to compare the quality of life and the anxiety-depression of patients according to their acceptance or refusal of the mixed care at the inclusion and at the end of the early phase trial, to compare the clinical, medical and socio-demographic characteristics of the patients, the overall survival of patients according to their acceptance or refusal of the combined management and finally for the patients accepting the PCM, to describe throughout the study, the patients' compliance to palliative supportive care undertaken.

All patients approached for inclusion in an early phase clinical trial during the Multidisciplinary Consultation Meeting (MCR) will be offered to participate to the study. In order to assess the reasons for accepting / refusing the inclusion in palliative supportive care in patients entering an early phase clinical trial, two subgroups will be formed. The first group will be made up of patients who accepts joint palliative care (n = 20) and the second group of those who refuse (n = 20). Following their acceptance, the consultation for setting up the early phase clinical trial will be recorded and participants will be invited to participate in a semi-structured interview just before the first line of treatment. Patients (both having accepted or refused the palliative care) will also have to answer a self-questionnaire on quality of life and anxiety-depression at inclusion and at the end of the clinical trial. The study results will make it possible to determine patients' motivations for accepting or refusing palliative care management in order to better define their expectations, beliefs in terms of management, their understanding and impact of this management.

Conditions
Cancer
Keywords
Cancer, Palliative care, Early phase trial
Medical subject headings
Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT04717440
Study groupRoleWhat they receive
Patients accepting palliative carePatients included in an early phase trial and accepting palliative care
Patients refusing palliative carPatients included in an early phase trial but refusing palliative care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Assessment of the reasons for accepting / refusing early palliative care in patients included in an early phase clinical trial

    Thematic content analysis of semi-directive qualitative interviews

    Measured: At baseline

Secondary outcomes (14)
  1. Description and analysis of the number (effective) of acceptance of early palliative support

    Numbers of acceptance of the early palliative care management for all patients seen in early phase unit consultation

    Measured: At baseline

  2. Description and analysis of the percentage of acceptance of early palliative support

    Percentages of acceptance of the early palliative care management for all patients seen in early phase unit consultation

    Measured: At baseline

  3. Assessment of patients' understanding and perception of the early palliative care management

    Comparison of qualitative semantic content of patient-investigator interaction with the semi-directive post-consultation inclusion interview

    Measured: At baseline

  4. Comparison of the quality of life of patients according to their acceptance or refusal of the mixed care

    Quality of life evaluated with the FACT-G7 (Functional Assessment of Cancer Therapy - General - 7-item version) questionnaire (range from 0 (better outcome) to 28 (worse outcome)

    Measured: Up to 24 months

  5. Comparison of the anxiety-depression of patients according to their acceptance or refusal of the mixed care

    Anxiety-depression evaluated with the HADS (Hospital Anxiety and Depression Scale) questionnaire (range 0-7: No symptoms, range 8-10: Doubtful symptoms, range >=11: Symptoms of anxiety or depression)

    Measured: Up to 24 months

  6. Comparison of the clinical, medical and socio-demographic characteristics of patients for the patients accepting the palliative care management

    Using PALLIA 10 scale (PALLIAtive scale composed of 10 items, minimum value: 1, maximum value: 10. A specialized advice in palliative care is required if score > 3)

    Measured: At baseline

  7. Comparison of the clinical, medical and socio-demographic characteristics of patients who accept or refuse the palliative care management

    Using PRONOPALL score (Prognostic overall survival score). Range 0-3: Favorable overall survival score, Range 4-7: Intermediate overall survival score, Range 8-10: Unfavorable overall survival score.

    Measured: At baseline

  8. Comparison of the clinical characteristics of patients who accept or refuse the palliative care management

    Clinical symptoms evaluated using ESAS (Edmonton Symptom Assessment System) questionnaire (range from 0 (better outcome) to 10 (worse outcome))

    Measured: At baseline

  9. Comparison of the socio-demographic characteristics of patients who accept or refuse the palliative care management

    Patients' characteristics (Age, sex, family situation, place of residence, socio-educational level, professional activity)

    Measured: At baseline

  10. Comparison of the medical characteristics of patients who accept or refuse the palliative care management

    Patients' medical history: Treatments

    Measured: Up to 24 months

  11. Comparison of the medical characteristics of patients who accept or refuse the palliative care management

    Patients' medical history: Use of specialists' consultations (e.g. intensive care unit, emergency hospitalization, palliative care unit, number/types of consultations, pain, nutrition)

    Measured: Up to 24 months

  12. Comparison of the use of social services of patients who accept or refuse the palliative care management

    Patients' medical history: Use of social service...

    Measured: Up to 24 months

  13. Overall survival of patients according to their acceptance or refusal of the "mixed" management

    Vital status

    Measured: Up to 24 months

  14. For patients having accepted the palliative support, description throughout the study of patients' compliance to palliative supportive care undertaken

    Patients having performed at least 50 percent of the visits

    Measured: Up to 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jan 2021
  2. Study start4 Feb 2021
  3. Primary completion22 Mar 2023
  4. Study completion22 Mar 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
37 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04717440
Sponsor's protocol ID
ET20-101 PALPHA-1
Acronym
PALPHA-1
Status last verified
Jul 2023
First submitted
10 Dec 2020
Last updated
13 Jul 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Chvetzoff G, Girodet M, Despax J, Baudry V, Duranti J, Mastroianni B, Vanacker H, Vinceneux A, Brahmi M, Renard O, Gautier J, Britel M, Ducimetiere F, Anota A, Cassier P, Christophe V. Reasons for acceptance and refusal of early palliative care in patients included in early-phase clinical trials in a regional comprehensive cancer centre in France: protocol for a qualitative study. BMJ Open. 2022 Apr 22;12(4):e060317. doi: 10.1136/bmjopen-2021-060317.

    PubMed 35459679

Questions about this trial

What is this clinical trial studying?

An observational study of Cancer, run by Centre Leon Berard at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Jul 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of the reasons for accepting / refusing early palliative care in patients included in an early phase clinical trial (time frame: At baseline). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04717440, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jul 2023.

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