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One-Minute Versus Two-Minute Compressor Rotation During Simulated Pediatric CPR (CPR-ROT)

2026年5月29日 更新者:Ahmet Ziya Birbilen、Hacettepe University

One-Minute Versus Two-Minute Compressor Rotation During Simulated Pediatric CPR: A Randomized Crossover Pilot Study

The goal of this clinical trial is to compare one-minute and two-minute compressor rotation intervals during simulated pediatric cardiopulmonary resuscitation, also called CPR. The study will include healthcare professionals who perform chest compressions on a pediatric manikin in a simulated resuscitation setting.

The main questions this study aims to answer are:

Does one-minute compressor rotation improve chest compression quality compared with two-minute compressor rotation? Does one-minute compressor rotation reduce participant fatigue compared with two-minute compressor rotation?

Participants will perform chest compressions during two simulated pediatric CPR sessions. In one session, compressors will rotate every one minute. In the other session, compressors will rotate every two minutes. Researchers will compare CPR performance measures and participant-reported fatigue between the two rotation intervals.

調査の概要

詳細な説明

This randomized crossover pilot study evaluates two different compressor rotation intervals during simulated pediatric cardiopulmonary resuscitation. The study is conducted in a simulation setting using a pediatric manikin. No patients are involved, and no clinical care is delivered.

Participants are healthcare professionals trained in pediatric resuscitation. Each participant pair completes two CPR scenarios. In one scenario, chest compressors rotate every one minute. In the other scenario, chest compressors rotate every two minutes. The order of the two scenarios is randomized.

The study compares objective CPR performance metrics obtained during the simulation, including measures related to chest compression quality. It also evaluates participant-reported fatigue after each scenario. Because each pair completes both rotation strategies, the crossover design allows comparison of the two approaches within the same participant pair.

The purpose of this pilot study is to explore whether a shorter compressor rotation interval may help maintain CPR quality or reduce fatigue during simulated pediatric CPR. The findings may help guide future simulation-based research and training strategies for pediatric resuscitation teams.

研究の種類

介入

入学 (実際)

18

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  • Volunteer pediatric residents
  • Previous cardiopulmonary resuscitation training
  • Prior clinical cardiopulmonary resuscitation experience
  • Ability to participate in both simulated pediatric CPR sessions
  • Written informed consent provided before study participation

Exclusion Criteria:

  • No previous Pediatric Advanced Life Support course attendance
  • No prior clinical cardiopulmonary resuscitation experience
  • Currently rotating in the pediatric emergency department or pediatric ward during the study period
  • Emergency medicine residents
  • Presence of a chronic medical condition that could affect physical performance during chest compressions

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:他の
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:One-Minute Then Two-Minute Rotation Sequence
Participants in this arm first performed simulated pediatric CPR with compressor rotation every one minute. After a rest period, they performed a second simulated pediatric CPR session with compressor rotation every two minutes.
During simulated pediatric cardiopulmonary resuscitation, chest compressors rotated every one minute. Participants performed chest compressions on a pediatric manikin, and CPR performance metrics were recorded during the simulation.
During simulated pediatric cardiopulmonary resuscitation, chest compressors rotated every two minutes. Participants performed chest compressions on a pediatric manikin, and CPR performance metrics were recorded during the simulation.
実験的:Two-Minute Then One-Minute Rotation Sequence
Participants in this arm first performed simulated pediatric CPR with compressor rotation every two minutes. After a rest period, they performed a second simulated pediatric CPR session with compressor rotation every one minute.
During simulated pediatric cardiopulmonary resuscitation, chest compressors rotated every one minute. Participants performed chest compressions on a pediatric manikin, and CPR performance metrics were recorded during the simulation.
During simulated pediatric cardiopulmonary resuscitation, chest compressors rotated every two minutes. Participants performed chest compressions on a pediatric manikin, and CPR performance metrics were recorded during the simulation.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Chest Compression Rate During Simulated Pediatric CPR
時間枠:From 0 to 20 minutes after the start of each simulated CPR session
Chest compression rate was recorded using a manikin-based CPR feedback device during each 20-minute simulated pediatric CPR session. The rate was compared between the one-minute and two-minute compressor rotation conditions.
From 0 to 20 minutes after the start of each simulated CPR session
Chest Recoil Velocity During Simulated Pediatric CPR
時間枠:From 0 to 20 minutes after the start of each simulated CPR session
Chest recoil velocity was recorded using a manikin-based CPR feedback device during each 20-minute simulated pediatric CPR session and compared between the one-minute and two-minute compressor rotation conditions.
From 0 to 20 minutes after the start of each simulated CPR session
Proportion of Adequate Chest Compressions
時間枠:From 0 to 20 minutes after the start of each simulated CPR session
The proportion of adequate chest compressions was defined as the proportion of compressions meeting the pre-specified rate and depth targets. Adequate compressions were defined as compressions delivered at a rate of 100 to 120 compressions per minute and a target depth of at least 5 cm
From 0 to 20 minutes after the start of each simulated CPR session

二次結果の測定

結果測定
メジャーの説明
時間枠
Participant-Reported Fatigue
時間枠:At 4, 8, 12, 16, and 20 minutes after the start of each simulated CPR session
Participant fatigue was assessed using a 10-point Likert-type fatigue scale. Scores range from 1 to 10, with 1 indicating the least fatigue and 10 indicating the most fatigue. Higher scores indicate worse fatigue. Fatigue scores were compared between the one-minute and two-minute compressor rotation conditions.
At 4, 8, 12, 16, and 20 minutes after the start of each simulated CPR session
Blood Pressure Response Before and After Simulated Pediatric CPR
時間枠:At baseline and immediately after completion of each simulated CPR session
Systolic and diastolic blood pressure were measured at baseline and at the end of each 20-minute simulated CPR session. Blood pressure responses were compared between the one-minute and two-minute compressor rotation conditions.
At baseline and immediately after completion of each simulated CPR session
Heart Rate Response During Simulated Pediatric CPR
時間枠:At baseline and at 4, 8, 12, 16, and 20 minutes after the start of each simulated CPR session
Participant heart rate was measured in beats per minute (bpm) using a standard monitor. Heart rate values were compared between the one-minute and two-minute compressor rotation conditions.
At baseline and at 4, 8, 12, 16, and 20 minutes after the start of each simulated CPR session

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出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年7月1日

一次修了 (実際)

2024年7月30日

研究の完了 (実際)

2024年9月1日

試験登録日

最初に提出

2026年5月21日

QC基準を満たした最初の提出物

2026年5月29日

最初の投稿 (実際)

2026年6月3日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月3日

QC基準を満たした最後の更新が送信されました

2026年5月29日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • SBA24-1093 (その他の識別子:Hacettepe University Health Sciences Research Ethics Committee)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

IPD プランの説明

The datasets generated and/or analyzed during the current study may be available from the corresponding author upon reasonable request, subject to approval by the study investigators and applicable institutional and ethical requirements.

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