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CompletedNCT02822690Updated Apr 19, 2024

Research Into the Quality of the Dying Phase

An observational study in Cessation of Life, sponsored by University Medical Center Groningen. Completed at 1 site in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-04-19.

Sponsored by University Medical Center Groningen · Observational

Study type
Observational
Model
Family-based
Time perspective
Prospective
Enrollment
200
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to get insight in the quality of life at the end of life and quality of dying for patients died at the hospital in the department Groningen (the Netherlands).

The primary endpoint is the quality of life at the end of life and the secondary endpoint is the quality of dying. Both according a numerical rating scale.

An explorative analysis will be done for differences for the hospitals in Groningen, effect of using the Liverpool care Pathway for the dying, effect of using consultation by the palliative consultation team, effect of using the Hospice@UMCG intervention, correlation with the quality of life at the end of life and quality of dying according to nurses and doctors.

Read the detailed description

Three hospitals in the department Groningen (the Netherlands) will participate in this study. When a patient died in one of these hospitals (except the emergency department, child ward and intensive care unit) the bereaved relatives will get an information letter. After about 12 weeks a questionnaire will be sent to the bereaved relative. This questionnaire is developed to evaluate the end of life care at the hospital.

Shortly after the patient died at the hospital, also the nurse and doctor of this patient are requested to fill out a questionnaire.

The questionnaire for the bereaved relatives consists of items, divided in groups: a general part, followed by questions of the last days of life, existing symptoms (physical, psychological, existential and social), the care and treatment and the loss.

The questionnaire for the nurses exists of similar items. Special attention for recognizing the impending dying and problems, care and therapy at the end of life.

In all questionnaires there are also 2 main questions: What is your opinion of the quality of life during the last days of life and What is your opinion of the quality of dying.

In the three hospitals the end of life care is managed at somehow different ways: the use of the Liverpool care Pathway of the dying, the hospice@UMCG intervention and consultation by the palliative team of the hospital.

02

Conditions studied

  • Cessation of Life

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Keywords

  • palliative care
  • Quality of dying
03

In context

Death

572 studies on the registry are indexed under Death; 111 are open to participants now.

This study's enrollment of 200 is below the median of 314 across 293 observational studies indexed under Death.

Browse Death studies →

Lead sponsor

University Medical Center Groningen is the lead sponsor of 609 studies on the registry; 174 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

all patients dying in the hospital

Inclusion criteria

  • patients dying in the hospital

Exclusion criteria

Exclusion Criteria:

  • patients dying at the child ward, emergency dept. and intensive care dept.
05

Study design

Observational model
Family-based
Time perspective
Prospective
Enrollment
200 participants (actual)
Patient registry
No

Groups and cohorts

  • University Medical Center Groningen

    all patients that died on one of the wards with the exception of children; on several wards the Hospice care will be introduced as an intervention

    Other: Hospice care at UMCG

  • Martini Ziekenhuis

    all patients that died on one of the wards with the exception of children

  • Ommelander ZorgGroep

    all patients that died on one of the wards with the exception of children

Interventions

  • OtherHospice care at UMCG

    introduction of hospice care facilities on the wards at the UMCG

06

What researchers measure

Primary outcomes

  1. Quality of life questionnaire

    Time frame: 2 years

07

Study locations

1 site
  • University Medical Center Groningen
    Groningen, 9713 GZ, Netherlands
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02822690
Lead sponsor
University Medical Center Groningen
Collaborators
Martini Hospital Groningen
Responsible party
Sponsor
First posted
Jul 4, 2016
Start date
Oct 2016
Primary completion
Jun 2019
Completion
Jun 2019
Last update
Apr 19, 2024

Study contacts

An KL Reyners, MD/PhD
principal investigator · UMCG

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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