NCT07292532 Learning Cardiopulmonary Resuscitation in the School Setting: RCP-KNOW Project.
| NCT ID | NCT07292532 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Castilla-La Mancha |
| Condition | Healthy Participants |
| Study Type | INTERVENTIONAL |
| Enrollment | 550 participants |
| Start Date | 2025-09-15 |
| Primary Completion | 2026-06-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 550 participants in total. It began in 2025-09-15 with a primary completion date of 2026-06-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
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.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07292532 clinical trial?
This trial is open to participants of all sexes, aged 5 Years or older, up to 13 Years, studying Healthy Participants. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07292532 currently recruiting?
Yes, NCT07292532 is actively recruiting participants. Contact the research team at dianap.pozuelo@uclm.es for enrollment information.
Where is the NCT07292532 trial being conducted?
This trial is being conducted at Cuenca, Spain, Cuenca, Spain.
Who is sponsoring the NCT07292532 clinical trial?
NCT07292532 is sponsored by University of Castilla-La Mancha. The trial plans to enroll 550 participants.