NCT07820605

Brief Summary

Cardiac arrest (CA) remains one of the leading causes of death worldwide, and its incidence continues to increase. The median survival rate following in-hospital cardiac arrest in France is 19%. In Europe, it ranges from 15% to 34%. Effective management of cardiac arrest is therefore essential to reduce the mortality rate associated with in-hospital cardiac arrest. However, cardiac arrest is a source of stress in conventional care settings. First, it is a life-threatening emergency in which the absence of effective management results in the patient's death. Furthermore, the occurrence of cardiac arrest in conventional hospital wards, particularly in pediatrics, is uncommon. Healthcare professionals are therefore not accustomed to encountering these situations, which may lead to apprehension, stress, and a lack of confidence in their skills when faced with cardiac arrest. In this context, maintaining skills is essential to ensure effective management of cardiac arrest. Providing open-access training in the workplace would make it possible to maintain a high level of proficiency over time while allowing healthcare professionals to remain at their workplace. The expected benefits are improved management of patients experiencing cardiac arrest through regular training and maintenance of the technical skills of paramedical and medical healthcare professionals in cardiopulmonary resuscitation (CPR). This is a retrospective cohort study evaluating the impact of a pre-/post-training intervention on the level of technical skills used by healthcare professionals in the management of cardiac arrest.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
265

participants targeted

Target at P75+ for all trials

Timeline
23mo left

Started Sep 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress5%
Sep 2026Sep 2028

First Submitted

Initial submission to the registry

August 28, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

September 15, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2028

Last Updated

September 15, 2026

Status Verified

September 1, 2026

Enrollment Period

2 years

First QC Date

August 28, 2026

Last Update Submit

September 14, 2026

Conditions

Keywords

RQICPRCPABVMSelf-trainingprocedural simulation

Outcome Measures

Primary Outcomes (1)

  • the success rate (total score greater than or equal to 75%) of RQI program participants

    the success rate (total score greater than or equal to 75%) of RQI program participants in order to evaluate the impact of the RQI self-training program on CPR technical skills

    12 months

Secondary Outcomes (11)

  • Success rate (score ≥ 75%) according to the number of logins to the station

    baseline and 12 months

  • Success rate (score ≥ 75%) according to the profession (Registered Nurse (RN), Nursing Assistant (NA), Physician)

    baseline and 12 months

  • Success rate (score ≥ 75%) according to Professional experience (number of years)

    baseline and 12 months

  • Success rate (score ≥ 75%) according to Department/unit of practice in order to evaluate of the Difference in Effectiveness of CPR Technical Skills According to Profile

    baseline and 12 months

  • Success rate (score ≥ 75%) according to occurrence of a cardiac arrest in the department in order to evaluate of the Difference in Effectiveness of CPR Technical Skills According to Profile

    baseline and 12 months

  • +6 more secondary outcomes

Eligibility Criteria

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

The study will include healthcare professionals working in one of the three departments of the A. Trousseau Children's Hospital: neonatal and pediatric intensive care, emergency department, and oncology/hematology.

You may qualify if:

  • \- Working in one of the 3 participating pediatric departments as a nursing assistant, nurse, physician, or healthcare manager

You may not qualify if:

  • \- Objection to the collection of his data

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

P₂ULSE

Paris, 75012, France

Location

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Léopoldine Legrain, Nurse

    Assistance Publique - Hôpitaux de Paris

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Léopoldine Legrain, nurse

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 28, 2026

First Posted

September 15, 2026

Study Start

September 1, 2026

Primary Completion (Estimated)

September 1, 2028

Study Completion (Estimated)

September 1, 2028

Last Updated

September 15, 2026

Record last verified: 2026-09

Locations