NCT04864613

Brief Summary

In our study, we aim to predict palliative care patients earlier, to reduce hospitalization periods and to prevent intensive care unit occupation by palliative care patients.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
135

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2019

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2019

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 8, 2020

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2020

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

January 30, 2021

Completed
3 months until next milestone

First Posted

Study publicly available on registry

April 29, 2021

Completed
Last Updated

April 29, 2021

Status Verified

April 1, 2021

Enrollment Period

1.1 years

First QC Date

January 30, 2021

Last Update Submit

April 25, 2021

Conditions

Palliative CareCritical CareLength of Stay

Outcome Measures

Primary Outcomes (1)

  • Recognition of palliative care unit patients before intensive care discharge

    ENDING-S Scoring system used to predict patients who were followed up in intensive care units and discharged to palliative care unit during their hospitalization. We aim to identify patients who are likely to be admitted to palliative care centers following their admission to intensive care units, and to prepare a palliative care center before the discharge from the intensive care.

    Fourth day of intensive care follow up

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Intensive care patients

You may qualify if:

  • Patients older than 18 years will be included in the study. Patients staying longer than 48 hours intensive care will be included in the study.

You may not qualify if:

  • Patients younger than 18 years. Patients staying less than 48 hours

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ministry of Health Ankara City Hospital

Ankara, 06800, Turkey (Türkiye)

Location

Study Officials

  • Işıl Özkoçak Turan, Prof.

    Ministry of Health Ankara City Hospital

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
30 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Specialist MD

Study Record Dates

First Submitted

January 30, 2021

First Posted

April 29, 2021

Study Start

June 1, 2019

Primary Completion

July 8, 2020

Study Completion

December 30, 2020

Last Updated

April 29, 2021

Record last verified: 2021-04

Data Sharing

IPD Sharing
Will not share

Locations

TU(1)