- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06310889
Evaluation of Palliative Care Co-treatment by Attending Physicians and Nurses: an Online Survey as Part of the Project (EPIC-BS)
Evaluation of Palliative Care Co-treatment by Attending Physicians and Nurses: an Online Survey as Part of the Project (EPIC-Baseline-Survey)
Study Overview
Status
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
Contacts and Locations
Study Locations
-
-
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Berlin, Germany, 13353
- Recruiting
- Department of Anesthesiology and Intensive Care Medicine (CCM/CVK), Charité - Universitätsmedizin Berlin
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Principal Investigator:
- Claudia Spies, MD
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Sub-Investigator:
- Andreas Edel, MD
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Contact:
- Claudia Spies, MD Prof.
- Phone Number: +49 30 531 012
- Email: claudia.spies@charite.de
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Principal Investigator:
- Sascha Tafelski, MD
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Sub-Investigator:
- Susanne Jöbges, MD
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Sub-Investigator:
- Christiane Hartog, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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).
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01.04.2024 - 30.06.2024
|
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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).
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01.04.2024 - 30.06.2024
|
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Measures 2
Time Frame: 01.04.2024 - 30.06.2024
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Evaluation of measures to be taken in the palliative medical treatment situation (family involvement in end-of-life-decisions).
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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
|
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Resources 2
Time Frame: 01.04.2024 - 30.06.2024
|
Other resources in palliative care (rate availability of psychological support)
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01.04.2024 - 30.06.2024
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Collaborators and Investigators
Collaborators
Investigators
- Study Chair: Claudia Spies, MD, Prof., Charite University, Berlin, Germany
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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