- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07646496
Comparison of Chest Compressions Performed With the Lower Limb and the Classical Method (Lower_limb_CPR). (Lower_limb_CPR)
Comparison of the Quality of Chest Compressions Performed With the Lower Limb and the Classical Method During Cardiopulmonary Resuscitation - a Simulation Study.
Chest compressions, alongside early defibrillation, are the most important component of basic life support for adults. High-quality compressions give the patient a chance to survive cardiac arrest.
The chest compression technique, described for years in guidelines, requires kneeling next to the victim and pressing down on the center of the chest with both extended arms at a specific rate and depth. However, there is a lack of scientific data on whether alternative compression methods (for example, using a lower limb) can be considered equally effective in situations where conventional compressions are impossible (e.g., the witness to cardiac arrest is a person with a disability, with an upper limb injury, or an elderly person; or when there is very little space to kneel). The aim of the study is to determine whether compressions performed with the dominant foot by paramedic and nursing students can be considered comparable in quality to conventional compressions. Furthermore, subjective levels of physical fatigue are assessed.
Participants are recruited from among paramedic and nursing students who voluntarily and knowingly consent to participate in the research study.
Inclusion Criteria
- Paramedic and nursing students from the Powiśle Academy of Applied Sciences who voluntarily and knowingly consent to participate in the study.
- Completed first aid training during their studies.
Exclusion Criteria
- Lack of consent to participate in the study.
- Education in another medical profession.
Procedure Students are randomly assigned to the control and study groups. Before participating in the simulation scenario, participants complete a questionnaire asking several demographic questions (age, gender, education, physical activity). Participants then enter the simulation room individually. The activities are not videotaped. From the moment of randomization, students are anonymous to the researcher. Both when completing the questionnaires and recording data from the simulation scenario, participants will be assigned a unique number (generated solely for the study), which prevents identification. Upon entering the simulation room, participants receive all instructions verbally. Students' task in the simulation environment involves performing two minutes of continuous chest compressions. Participants in the control group perform these compressions traditionally, while those in the study group are asked to perform compressions using their dominant leg. Compression quality is assessed using a Prestan Manikin (2000 series) with the CPR FEEDBACK mobile app. Parameters such as compression depth, rate, and relaxation are assessed. Completion of chest compressions on the manikin marks the end of the simulation scenario. Furthermore, participants are verbally questioned after the simulation about their level of physical fatigue on a scale of 1 (none) to 10 (the most severe ever).
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Pomeranian Voivodeship
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Kwidzyn, Pomeranian Voivodeship, Polen, 82-500
- Powiślańska Academy of Applied Sciences
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria
- Paramedic and nursing students from the Powiśle Academy of Applied Sciences who voluntarily and knowingly consent to participate in the study.
- Completed first aid training during their studies.
Exclusion Criteria
- Lack of consent to participate in the study.
- Education in another medical profession.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Ingen indgriben: Styring
|
|
|
Eksperimentel: Undersøgelse
|
Verbal instruction to perform chest compressions using the lower limb (foot) before the simulation scenario.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Chest compressions quality - Frequency
Tidsramme: 2 minutes
|
2 minutes
|
|
Chest compressions quality - Relaxation
Tidsramme: 2 minutes
|
2 minutes
|
|
Chest compressions quality - Depth
Tidsramme: 2 minutes
|
2 minutes
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Fatigue
Tidsramme: 2 minutes
|
Self-assessed physical fatigue (1-10 scale)
|
2 minutes
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Powiślańska1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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