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Palliative CareNOVOPALNCT07505706

Patient Journey in Palliative Care Within the NOVO Hospital Group.

An observational study of Palliative Care and End of Life Care, run by Hôpital NOVO 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 retrospective descriptive study aims to describe the sociodemographic, clinical, and organizational characteristics of patients identified as receiving palliative care who died in 2024 within the NOVO Hospital network. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Palliative Care, End of Life Care, Terminal Care
How many people
286 participants
Where
1 siteFrance
Study dates
5 Jan 2026to 31 Mar 2026
Phase
Observational

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: Patients who died between January 1, 2024, and December 31, 2024, in the hospital or in their personal living space (home, nursing home...)

Who may be able to join

  • Patients who died between January 1, 2024, and December 31, 2024, in the hospital or in their personal living space (home, nursing home...)
  • Having "palliative care" status in their medical record
  • Receiving care at one of the six NOVO hospital sites (Pontoise, Magny-en-Vexin, Beaumont-sur-Oise, Marines, Saint-Martin-du-Tertre, Aincourt)
  • Whether or not they were followed by a mobile palliative care team

Who cannot join

  • None

Trial locations and contacts

1 site in 1 country.

France1 site
  • Hospital Novo

    Pontoise, 95300

Other trials in France

About this study

Official title: A Descriptive and Analytical Study of Patients Who Died in 2024 While Receiving Palliative Care at NOVO Hospital: Patient Characteristics and Implications for General Practice?

This retrospective descriptive study aims to describe the sociodemographic, clinical, and organizational characteristics of patients identified as receiving palliative care who died in 2024 within the NOVO Hospital network.

Data from medical records will include patient characteristics, involvement of general practitioners, use of palliative care services, healthcare utilization, and conditions of death.

The study hypothesizes that improved characterization of these patients and their care trajectories will help identify opportunities for earlier palliative care referral and better coordination between hospital and community care.

Read the detailed description

Population aging and the increasing prevalence of chronic diseases and frailty have led to a growing demand for palliative care. End-of-life trajectories are frequently complex and involve multiple transitions between hospital care, home, and long-term care facilities. In many healthcare systems, a large proportion of healthcare expenditures in the last months of life is related to hospitalizations. A better understanding of the characteristics and care pathways of patients receiving palliative care is therefore essential to improve the organization and coordination of end-of-life care.

In France, general practitioners play a key role in the follow-up of patients and in coordinating care between hospital and community settings. However, the identification of palliative care needs and the timing of referral to specialized palliative care services remain heterogeneous. Improved knowledge of patient profiles and care trajectories may help identify opportunities to strengthen collaboration between hospital teams and primary care physicians.

This retrospective monocentric descriptive study will analyze patients identified as receiving palliative care who died in 2024 within the NOVO Hospital network. Data will be extracted from the medical record system and anonymized prior to analysis.

Collected variables will include sociodemographic characteristics, clinical information such as comorbidities, level of autonomy, and data related to the organization of care. Particular attention will be given to the involvement of general practitioners, the use of specialized palliative care teams, and access to home-based care services. The study will also examine healthcare utilization in the last months of life, including hospital admissions and emergency department visits, as well as end-of-life conditions such as the place of death, the presence of advance directives, and the use of continuous deep sedation.

By describing patient profiles and care trajectories, this study aims to identify potential factors associated with healthcare utilization and to highlight opportunities to improve early palliative care identification and coordination between hospital and community care.

Keywords
Palliative Care, End of Life Care, Primary Health Care, General Practitioners, Care Coordination, Place of Death, Advance Directives, Health Services Utilization, Retrospective Studies
Medical subject headings
Patient Acceptance of Health Care

What is being measured

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

  1. Number and profiles of patients identified as receiving palliative care who died in 2024 within the NOVO Hospital network

    Description of the sociodemographic, clinical, and organizational characteristics of patients identified as receiving palliative care, including age, sex, living situation, level of autonomy, primary disease, comorbidities, presence of advance directives, and existence of a documented care plan.

    Measured: Through study completion, an average of 3 months

Secondary outcomes (5)
  1. Place of death and concordance with patient preferences

    Assessment of the actual place of death (hospital, home, nursing home or other setting) and comparison with the place of death expressed in advance directives or documented care plans when available

    Measured: Through study completion, an average of 3 months

  2. Involvement of general practitioners in palliative care management

    Evaluation of the presence of a primary care physician and their involvement in the patient's palliative care pathway, including participation in care planning and coordination with hospital teams

    Measured: Through study completion, an average of 3 months

  3. Healthcare utilization in the last months of life

    Number of hospital admissions and emergency department visits during the last six months of life

    Measured: At the end of the study, an average of 3 months

  4. Timing of referral to palliative care

    Time interval between the identification of a palliative situation and the first contact with palliative care services.

    Measured: Through study completion, an average of 3 months

  5. Explore ways to improve the early identification of palliative care needs and ensure continuity of care between home and hospital

    Time between the date of death and the start of palliative care

    Measured: Through study completion, an average of 3 months

Timeline

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

  1. First posted1 Apr 2026
  2. Study start5 Jan 2026
  3. Primary completion31 Mar 2026
  4. Study completion31 Mar 2026

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
Retrospective
Enrolment
286 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07505706
Sponsor's protocol ID
CHRD1825
Other IDs
CHRD1825
Acronym
NOVOPAL
Status last verified
Sep 2026
First submitted
18 Mar 2026
Last updated
17 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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