NCT06425692

Brief Summary

The EPIC project aims at sustainably improving palliative care for seriously ill patients and their families in ICUs. To this aim, an interdisciplinary consortium is working together to provide a new practical palliative care model using telemedicine. The project is the first European intervention study on palliative care in the ICU using a systems- based approach with proactive patient identification, checklist and blended learning designed to meet the specific needs of ICU staff. EPIC's vision is to contribute to a change in awareness from a narrow focus on prolonging life to a more holistic approach to care. The development of blended learning for intensive care staff is the task of Work Package (WP) 3. The aim is to improve the attitude, understanding and self-confidence of ICU staff. Blended learning is to be developed and implemented for this purpose. The aim is to teach the basics of palliative care on a cognitive, affective and psychomotor level. Due to the international character of the project, it is to be developed in English with subtitles in the local languages. In addition a workshop with patient and family advisors will be conducted.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
500

participants targeted

Target at P75+ for not_applicable

Timeline
33mo left

Started Sep 2024

Longer than P75 for not_applicable

Status
not yet recruiting

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 Progress39%
Sep 2024Jan 2029

First Submitted

Initial submission to the registry

May 1, 2024

Completed
21 days until next milestone

First Posted

Study publicly available on registry

May 22, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
3.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2028

Expected
10 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2029

Last Updated

May 22, 2024

Status Verified

May 1, 2024

Enrollment Period

3.5 years

First QC Date

May 1, 2024

Last Update Submit

May 21, 2024

Conditions

Keywords

multi-center studyICU staffEU-Horizon

Outcome Measures

Primary Outcomes (2)

  • CSA-gain

    The comparative self-assessment (CSA) gain is used to evaluate the specific learning effects in relation to the increase in knowledge, attitudes and skills \[2\]. Here, the participants assess their own increase in knowledge in the post/this assessment. The information is assessed using german school grades (1 = very good, 6 = unsatisfactory). Subsequently, the learning gain on the levels of attitude and knowledge can be calculated as "Comparative Self-Assessment Gain" (CSA Gain \[%\] = ((MWpre- MWpost)/(Mwpre-1)) x 100) using specific outcome evaluation.

    e-Learning: 45 minutes, CSA-gain immediately after e-learning and 6 months post e-learning.

  • CPD Response Questionnaire ("Continuing professional development")

    12-item questionnaire to assess the impact of CPD activities on changes in clinical behavioural intentions

    Right before starting the 45-minute e-learning session + immediately after the completion of one of the offered online workshops (to be held on two Thursdays per month for 5 years) + 6 months post blended learning.

Study Arms (1)

Education on basic palliative care

OTHER

Blended learning for ICU staff and online webinars. The aim is to teach the basics of palliative care on a cognitive, affective and psychomotor level.

Behavioral: Education

Interventions

EducationBEHAVIORAL

Education on basic palliative care via e-learning + webinar to deepen knowledge.

Education on basic palliative care

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • ≥18 years
  • ICU staff and participants of the EPIC intervention study (physician, nurse)
  • participants of patients and family workshops
  • agreement to participate in the study

You may not qualify if:

  • \<18 years
  • rejection of study participation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Raupach T, Munscher C, Beissbarth T, Burckhardt G, Pukrop T. Towards outcome-based programme evaluation: using student comparative self-assessments to determine teaching effectiveness. Med Teach. 2011;33(8):e446-53. doi: 10.3109/0142159X.2011.586751.

    PMID: 21774642BACKGROUND
  • Legare F, Freitas A, Turcotte S, Borduas F, Jacques A, Luconi F, Godin G, Boucher A, Sargeant J, Labrecque M. Responsiveness of a simple tool for assessing change in behavioral intention after continuing professional development activities. PLoS One. 2017 May 1;12(5):e0176678. doi: 10.1371/journal.pone.0176678. eCollection 2017.

    PMID: 28459836BACKGROUND

MeSH Terms

Interventions

Educational Status

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SEQUENTIAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 1, 2024

First Posted

May 22, 2024

Study Start

September 1, 2024

Primary Completion (Estimated)

March 1, 2028

Study Completion (Estimated)

January 1, 2029

Last Updated

May 22, 2024

Record last verified: 2024-05