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Hand Position, CPR Quality and Rescuer Comfort

2026년 9월 11일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

100

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

예

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 크로스오버 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
활성 비교기: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Mean chest compression depth (mm)
기간: During procedure.
Mean chest compression depth recorded continuously by the manikin's integrated measurement system during CPR performance.
During procedure.

2차 결과 측정

결과 측정
측정값 설명
기간
Chest compression rate (per minute)
기간: 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 (%)
기간: 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 (%)
기간: 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)
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Bálint Bánfai, PhD, University of Pécs Faculty of Health Sciences

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 10월 15일

기본 완료 (추정된)

2027년 2월 15일

연구 완료 (추정된)

2027년 3월 15일

연구 등록 날짜

최초 제출

2026년 9월 11일

QC 기준을 충족하는 최초 제출

2026년 9월 11일

처음 게시됨 (실제)

2026년 9월 17일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 17일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 11일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • CPR hand position

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

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아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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