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Practices of Accompaniment of the Relatives of Patients in the AGonic Phase by an Interdisciplinary Team (PROPAGE2)

U

University Hospital of Bordeaux

Status

Completed

Conditions

Practice Nurse's Scope

Treatments

Other: questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT04818684
CHUBX 2019/60

Details and patient eligibility

About

The PROPAGE study program aims above all to improve the experience and satisfaction of family and friends regarding the support they receive during the dying person's agony phase.

Full description

The objective of PROPAGE 2 is to establish a consensus on the practices for accompanying relatives during the agonic phase in the context of hospitalization in the palliative care unit by an interdisciplinary team.

Enrollment

278 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

INCLUSION CRITERIA

  1. PALLIATIVE CARE UNITS (USP) 35 palliative care unit will be drawn at random among the 164 French palliative care unit (www.sfap.org). In the event of refusal of participation, the drawing of lots will continue until 35 participating palliative care unit are obtained. The inclusion criteria for palliative care units were determined from the survey carried out in 2013 by the National End of Life Observatory on palliative care units in France. In order for there to be representativeness, the status of the palliative care unit will be taken into account from the national University Hospital (CHU) distribution, excluding CHU in the public sector, private non-profit sector, private for-profit sector. Thus, out of the 35 palliative care units: 7 will be within CHU, 16 will be outside CHU in the public sector, 7 will be in the private non-profit sector, and 5 in the private for-profit sector (criteria determined from the survey of the National End of Life Observatory in 2013) by ensuring that there are no more than 3 palliative care units in the same department (this in order to avoid that a geographical territory is over-represented, which would be liable to bias the results).

    In the event of refusal of a palliative care units or of inadequacy of the criteria, the drawing of lots will be continued until 35 participating USPs are obtained.

    Each team of these palliative care units must allow the participation of 7 experts: 1 for each group of experts, i.e. 5 socio-health professionals working in all the palliative care units (doctors, psychologists, nursing assistants, nurses, socio-educational assistant) as well as the coordinator of support volunteers and a relative by palliative care unit.

  2. THE EXPERTS

6 volunteer experts who will participate in the panel of voters: a doctor (group 1), an IDE ( group 2), an AS (group 3), a psychologist (group 4), an ASE (group 5), a volunteer support coordinator (group 6) . A relative (group 7) will be done.

The inclusion criteria:

  • For professionals, at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit.
  • For volunteers, at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit. The representative participating in the study will preferably be the volunteer coordinator.
  • For relatives Relative of a patient who died in the palliative care unit at least 6 months ago Person to trust or to prevent if not designated Relative understanding and speaking sufficient French Relative not a health professional

Relative who visited the palliative care unit during the last 3 days of the patient's life and who met the care team:

  • Traceability of the arrival of the loved one in the last 2/3 days of the patient's hospitalization
  • Traceability of a meeting of the loved one with a member of the team over the last 3 days of his hospitalization or verification during telephone contact with the loved one after drawing lots Relative with an email address (to be verified during telephone contact with the loved one after drawing lots)

NO-INCLUSION AND EXCLUSION CRITERIA

  1. PALLIATIVE CARE UNITS Palliative care unit who could not be represented by the 7 experts required

    • Have participated in the PROPAGE 1 study
    • Have taken part in the questionnaire test.
  2. THE EXPERTS Palliative care unit Experts: Anyone with less than 3 years of palliative care unit experience.

Relatives:

Relative of a patient who died in the palliative care unit less than 6 months ago Relative not understanding and not speaking French enough Relative being a health professional Relative who has not been to the palliative care unit in the last 3 days of the patient's life Relative who does not have an email address (to be checked during telephone contact with the loved one after drawing lots).

Trial design

278 participants in 7 patient groups

Physician
Description:
at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit.
Treatment:
Other: questionnaire
Psychologists
Description:
at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit.
Treatment:
Other: questionnaire
Caregivers
Description:
at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit.
Treatment:
Other: questionnaire
Nurses
Description:
at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit.
Treatment:
Other: questionnaire
Social and Educational Assistants
Description:
at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit.
Treatment:
Other: questionnaire
Volunteers
Description:
at least 3 years of seniority in palliative care unit will be required, including 1 year in the participating palliative care unit. The representative participating in the study will preferably be the volunteer coordinator.
Treatment:
Other: questionnaire
Relatives
Description:
Relative of a patient who died in the palliative care unit at least 6 months ago Person to trust or to prevent if not designated Relative understanding and speaking sufficient French Relative not a health professional Relative who visited the palliative care unit during the last 3 days of the patient's life and who met the care team: * Traceability of the arrival of the loved one in the last 2/3 days of the patient's hospitalization * Traceability of a meeting of the loved one with a member of the team over the last 3 days of his hospitalization or verification during telephone contact with the loved one after drawing lots Relative with an email address (to be verified during telephone contact with the loved one after drawing lots)
Treatment:
Other: questionnaire

Trial contacts and locations

1

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Central trial contact

Maïder MÉLIN; Carole ROUMIGUIERE

Data sourced from clinicaltrials.gov

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