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Hand Position, CPR Quality and Rescuer Comfort

11 de septiembre de 2026 actualizado por: Dr. Bálint Bánfai, University of Pecs

Effect of Hand Position During Chest Compressions on Resuscitation Quality and Rescuer Comfort: A Randomized Crossover Simulation Study

This randomized crossover simulation study will compare two hand positions used during chest compressions: interlocked fingers and non-interlocked hands placed one on top of the other. The study will evaluate whether the non-interlocked hand position is non-inferior to the interlocked-finger technique with regard to chest compression depth, and will compare the two techniques in terms of CPR quality, rescuer comfort, fatigue, pain or discomfort, and perceived hand-position stability.

Descripción general del estudio

Descripción detallada

High-quality chest compressions are a key component of cardiopulmonary resuscitation (CPR). Current international resuscitation guidelines recommend placing one hand on top of the other during chest compressions, but recommendations regarding whether the fingers should be interlocked or simply placed on top of each other are based on limited scientific evidence.

This prospective, randomized, controlled crossover simulation study will compare two hand positions during continuous chest compressions on an adult CPR manikin. Each participant will perform two 2-minute chest compression periods, using both techniques in a computer-randomized order: (1) interlocked fingers, representing the commonly taught technique, and (2) non-interlocked hands placed one on top of the other. A 10-minute seated rest period will separate the two measurement periods.

The primary outcome will be mean chest compression depth. Secondary outcomes will include compression rate, proportion of compressions with adequate depth and full chest recoil, temporal changes in compression depth, and subjective assessments of pain, discomfort, physical fatigue, hand-position stability, and confidence in performing chest compressions. Participants will also indicate which technique they would prefer in a real resuscitation situation.

The study will be conducted in a simulation environment at the Human Patient Simulation Center of the University of Pécs Faculty of Health Sciences. Participants will not receive real-time feedback from the manikin during the measurements.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

100

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Pécs, Hungría, 7621
        • Reclutamiento
        • University of Pecs
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Adults aged 18 years or older
  • Healthcare professionals or laypersons
  • Physically able to perform chest compressions
  • Able and willing to provide written informed consent to participate in the study

Exclusion Criteria:

  • Acute injury of the upper extremities
  • Chronic musculoskeletal disease or symptoms that may interfere with the ability to perform chest compressions with adequate quality
  • technical issue during data collection

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Interlocked fingers
Participants will perform continuous chest compressions using the interlocked-finger hand position. One hand will be placed on the lower half of the sternum, with the other hand placed on top and the fingers interlocked. Chest compressions will be performed for 2 minutes according to current international CPR recommendations, targeting a compression depth of 5-6 cm, a rate of 100-120 compressions per minute, and complete chest recoil after each compression. No real-time feedback from the manikin will be provided during the measurement.
Participants will perform chest compressions using the interlocked-finger hand position. One hand will be placed on the lower half of the sternum and the other hand on top, with the fingers interlocked. The intervention will consist of 2 minutes of continuous chest compressions performed at a target rate of 100-120 compressions per minute and a target depth of 5-6 cm, with complete chest recoil after each compression. No real-time feedback will be provided.
Comparador activo: Overlapped hands
Participants will perform continuous chest compressions using the non-interlocked hand position. One hand will be placed on the lower half of the sternum, with the other hand placed directly on top without interlocking the fingers. Finger contact between the two hands will be permitted, but active interlocking will not be performed. Chest compressions will be performed for 2 minutes under the same conditions as the interlocked-finger condition, targeting a compression depth of 5-6 cm, a rate of 100-120 compressions per minute, and complete chest recoil after each compression. No real-time feedback from the manikin will be provided during the measurement.
Participants will perform chest compressions using the non-interlocked hand position. One hand will be placed on the lower half of the sternum and the other hand on top without interlocking the fingers. The intervention will consist of 2 minutes of continuous chest compressions performed under the same conditions as the interlocked-finger technique, with a target rate of 100-120 compressions per minute, a target depth of 5-6 cm, and complete chest recoil after each compression. No real-time feedback will be provided.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Mean chest compression depth (mm)
Periodo de tiempo: During procedure.
Mean chest compression depth recorded continuously by the manikin's integrated measurement system during CPR performance.
During procedure.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Chest compression rate (per minute)
Periodo de tiempo: During procedure.
Mean chest compression rate (compressions per minute) recorded by the manikin's integrated measurement system during CPR performance.
During procedure.
Proportion of compressions with adequate depth (%)
Periodo de tiempo: During procedure.
Proportion of chest compressions meeting the predefined target depth, as recorded by the manikin's integrated measurement system.
During procedure.
Proportion of compressions with complete chest recoil (%)
Periodo de tiempo: During procedure.
Proportion of chest compressions followed by complete chest recoil, as recorded by the manikin's integrated measurement system.
During procedure.
Interruption duration (sec)
Periodo de tiempo: During procedure.
Duration of interruptions in chest compressions (hand-off time), if applicable, recorded by the manikin's integrated measurement system.
During procedure.
Overall chest compression quality score (points, mean, SD)
Periodo de tiempo: During procedure.
Overall chest compression quality score calculated by the manikin's integrated measurement system based on predefined CPR performance parameters.
During procedure.
Self-reported hand pain
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' self-reported overall hand pain following CPR performance, assessed using a 0-10 Numeric Rating Scale, where 0 indicates no pain and 10 indicates the worst imaginable pain.
Immediately after the CPR procedure (within 15 minutes)
Finger discomfort
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' self-reported discomfort in the fingers following CPR performance, assessed using a 0-10 Numeric Rating Scale.
Immediately after the CPR procedure (within 15 minutes)
Wrist discomfort
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' self-reported wrist discomfort following CPR performance, assessed using a 0-10 Numeric Rating Scale.
Immediately after the CPR procedure (within 15 minutes)
Perceived physical fatigue
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' self-reported physical fatigue following CPR performance, assessed using a 0-10 Numeric Rating Scale.
Immediately after the CPR procedure (within 15 minutes)
Perceived hand-position stability
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' perceived stability of their hand position during CPR performance, assessed using a 0-10 Numeric Rating Scale.
Immediately after the CPR procedure (within 15 minutes)
Perceived hand slippage
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' perceived sensation of hand slippage during CPR performance, assessed using a 0-10 Numeric Rating Scale.
Immediately after the CPR procedure (within 15 minutes)
Preferred hand position
Periodo de tiempo: Immediately after the CPR procedure (within 15 minutes)
Participants' preferred hand position for performing CPR in a real-life cardiac arrest situation.
Immediately after the CPR procedure (within 15 minutes)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Bálint Bánfai, PhD, University of Pécs Faculty of Health Sciences

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

15 de octubre de 2026

Finalización primaria (Estimado)

15 de febrero de 2027

Finalización del estudio (Estimado)

15 de marzo de 2027

Fechas de registro del estudio

Enviado por primera vez

11 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

11 de septiembre de 2026

Publicado por primera vez (Actual)

17 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

11 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • CPR hand position

Plan de datos de participantes individuales (IPD)

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INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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