MedPath

Evaluation of End of Life Quality of Care

Completed
Conditions
End of Life Care
Neoplasm Malignant
Quality of Life
Registration Number
NCT03775304
Lead Sponsor
Assistance Publique - H么pitaux de Paris
Brief Summary

The study uses a mixed method study to evaluate wether the use of the indicators of the Quality of end-of-life cancer care, developed by Earle et al \[Earle JCO 2003; DOI: 10.1200/JCO.2003.03.059\] would be relevant and measurable in France. The qualitative part of study was designed to investigate the representations of quality by face-to face interviews with family carer of recently deceased cancer patients, and with their oncologists, and nurses. The quantitative part of the study, consisted in a decedents case series analysis, diagnosed with advanced cancer and followed up in 5 centers. Data on trajectory of care were collected from different complementary sources associating national mortality data, hospital activity data, and health records.

The study was approved by the French data protection authority (CNIL) number 611273.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
997
Inclusion Criteria

Not provided

Exclusion Criteria
  • diagnosis with non solid tumor (haematology)
  • age < 18

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Use of emergency services within last 30 days before deathThrough study completion, up to 1 year
Secondary Outcome Measures
NameTimeMethod
Admission in intensive care unit within last 30 days before deathThrough study completion, up to 1 year
Location of deathThrough study completion, up to 1 year
Among patients with pain relief opioid treatment, those with combined short term and long acting opioid ordersThrough study completion, up to 1 year
Patients received chemotherapy in the last 14 days of lifeThrough study completion, up to 1 year
Among patients who died in palliative care unit, those who died within 3 days after admissionThrough study completion, up to 1 year

Trial Locations

Locations (5)

APHP H么pital Cochin

馃嚝馃嚪

Paris, France

APHP H么pital Henri Mondor

馃嚝馃嚪

Paris, France

Institut Curie

馃嚝馃嚪

Paris, Ile De France, France

Institut Gustave Roussy

馃嚝馃嚪

Villejuif, France

APHP H么pital Europ茅en Georges Pompidou

馃嚝馃嚪

Paris, France

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