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Recruiting NCT07292532

Learning Cardiopulmonary Resuscitation in the School Setting: RCP-KNOW Project.

No phase Interventional Healthy Participants Knowledge Acquisition Cardiopulmonary Resuscitation (CPR) Children

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cardiopulmonary Resuscitation Teaching Intervention in Children.
Who it may be relevant to
Registry conditions: Healthy Participants, Knowledge Acquisition, Cardiopulmonary Resuscitation (CPR), Children. Basic parameters: 5 years — 13 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Spain
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Out-of-hospital Cardiorespiratory Arrest and Learning Cardiopulmonary Resuscitation in the School Setting: Evidence Synthesis

Overview

Title: Out-of-hospital cardiorespiratory arrest and learning cardiopulmonary resuscitation in the school setting: evidence synthesis. CPR-KNOW PROYECT. Background: The high incidence, associated morbidity and mortality, and the great individual, social and economic impact of out-of-hospital cardiorespiratory arrest (OHCA) make it a priority for all health systems worldwide. To increase the rates of potential first responders who act appropriately, applying basic life support (BLS) measures in the OHCA, the European Resuscitation Council includes among its latest recommendations the training of all school children through the "Kids Save Lives" initiative. Objectives: to determine, through a randomized clinical trial, the effectiveness of two training strategies for increasing theoretical and practical knowledge of BLS in schoolchildren and adolescents. Methodology: To evaluate the effectiveness of two (Cardiopulmonary Resuscitation) CPR teaching interventions in improving the following outcome variables: theoretical knowledge and practical skills, CPR quality; as well as its relationship with the anthropometric, sociodemographic and physical condition variables of the schoolers. * Intervention group 1 (IG1): a 2-hour theoretical-practical session on the BLS sequence taught by a Nursing professional performing the practice with a mannequin. Instructor/school ratio: 1/25 for the theoretical session and a school/mannequin ratio: 2-3/1. * Intervention group 2 (IG2): a session with short video (approximately 5-10 min) and other teaching resources (puzzle), without practice on a mannequin. Video/school ratio: 1/25 and a school/teaching resource (puzzle) ratio: 1/1.

Interventions

  • Other Cardiopulmonary Resuscitation Teaching Intervention in Children
    Comparation of two type of Cardiopulmonary Resuscitation Teaching Intervention in Children: traditional teaching vs video with puzzle.

Primary outcome measures

  • Theoretical CPR Knowledge [Time frame: On the same day as the intervention, before (pre-intervention) and immediately after this (post-intervention) and follow-up (8 months later)]
  • CPR Practice Skills [Time frame: On the same day as the intervention immediately after this (post-intervention) and follow-up (8 months later)]
  • Quality of CRP [Time frame: On the same day as the intervention, immediately after this (post-intervention) and follow-up (8 months later)]

Eligibility criteria

Inclusion criteria

  • Schools that have at least one complete year of 1st, 2nd, 3rd, 4th, 5th and 6th year of Primary Education, in which the School Council has given its approval for their participation.
  • Schoolchildren who wish to participate must:
  • Belong to the courses from 1st to 6th grade of Primary Education
  • Understand the written and spoken Spanish language
  • Not have any physical, mental or cognitive pathology that prevents them from participating in the project.
  • Their father/mother or guardian must have signed the informed consent to be able to participate in the project.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Spain · 2 centers
  • CEIP Ciudad Encantada — Cuenca
  • CEIP Isaac Albeniz — Cuenca

Identifiers

NCT: NCT07292532 · SBPLY/23/180225/000060 · SBPLY/23/180225/000060

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗