Evaluation of Palliative Care Co-treatment by Attending Physicians and Nurses: an Online Survey as Part of the Project (EPIC-BS)

March 15, 2024 updated by: Claudia Spies, Charite University, Berlin, Germany

Evaluation of Palliative Care Co-treatment by Attending Physicians and Nurses: an Online Survey as Part of the Project (EPIC-Baseline-Survey)

The subject of the study is an online survey of doctors and nurses who provide (intensive) medical care to patients.

Study Overview

Status

Withdrawn

Conditions

Detailed Description

Charité will support this international survey as part of the preparatory phase of the "Europe-wide harmonized and recommended palliative care practice for ICU" approved HORIZON grant application EPIC (EA2/291/23), to which this ethics application refers.

Participants will be contacted via the mailing list of ESAIC (European Organization for Anaesthesia, Intensive Care, Pain and Perioperative Medicine), ESICM (European Society of Intensive Care Medicine), DIVI (German Interdisciplinary Association for Intensive Care and Emergency Medicine (DIVI) and the European Association for Palliative Care (EAPC).

Study Type

Observational

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Berlin, Germany, 13353
        • Recruiting
        • Department of Anesthesiology and Intensive Care Medicine (CCM/CVK), Charité - Universitätsmedizin Berlin
        • Principal Investigator:
          • Claudia Spies, MD
        • Sub-Investigator:
          • Andreas Edel, MD
        • Contact:
        • Principal Investigator:
          • Sascha Tafelski, MD
        • Sub-Investigator:
          • Susanne Jöbges, MD
        • Sub-Investigator:
          • Christiane Hartog, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Doctors or nursing staff involved in the intensive medical care of patients which can be contacted by a list of a specialist association

Description

Inclusion Criteria:

  • All doctors or nursing staff involved in the intensive medical care of patients and consent to the survey via the distribution list of a specialist association

Exclusion Criteria:

  • Incomplete data

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Barriers 1
Time Frame: 01.04.2024 - 30.06.2024
Barriers in palliative care regarding implementation of therapeutic goals (implementation rate symptom assessment for e.g. breathing and dyspnea).
01.04.2024 - 30.06.2024
Barriers 2
Time Frame: 01.04.2024 - 30.06.2024
Barriers in palliative care regarding implementation of patient automomy (implementation rate to define advance directives and power of attorney).
01.04.2024 - 30.06.2024

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measures 1
Time Frame: 01.04.2024 - 30.06.2024
Measures to be taken in the palliative medical treatment situation (implementation rate to define and document end-of-life-decisions).
01.04.2024 - 30.06.2024
Measures 2
Time Frame: 01.04.2024 - 30.06.2024
Evaluation of measures to be taken in the palliative medical treatment situation (family involvement in end-of-life-decisions).
01.04.2024 - 30.06.2024
Resources 1
Time Frame: 01.04.2024 - 30.06.2024
Personnel resources in palliative care (rate of specialized palliative care team available in ICUs).
01.04.2024 - 30.06.2024
Resources 2
Time Frame: 01.04.2024 - 30.06.2024
Other resources in palliative care (rate availability of psychological support)
01.04.2024 - 30.06.2024

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Claudia Spies, MD, Prof., Charite University, Berlin, Germany

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 1, 2024

Primary Completion (Estimated)

June 30, 2024

Study Completion (Estimated)

June 30, 2024

Study Registration Dates

First Submitted

February 22, 2024

First Submitted That Met QC Criteria

March 12, 2024

First Posted (Actual)

March 15, 2024

Study Record Updates

Last Update Posted (Actual)

March 18, 2024

Last Update Submitted That Met QC Criteria

March 15, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • EPIC-Baseline-Survey

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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