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Effectiveness of a Communication Training Program in Improving the Handling of Calls for Suspected Cardiac Arrest at SAMU-Centre 15. (COM-ARM)

2026年8月17日 更新者:University Hospital, Grenoble

Effectiveness of a Communication Training Program in Improving the Handling of Calls for Suspected Cardiac Arrest at SAMU-Centre 15. A Multicenter, Randomized Controlled Stepped-Wedge Implementation Trial

Each year, France's emergency response services-the SAMU (15) and the fire department (18)-handle 31 million and 19 million calls, respectively. The effectiveness of this system depends on the call centers' ability to obtain location information, prioritize responses, assess the severity of each call, and dispatch appropriate emergency resources.

Cardiac arrest (CA) affects 40,000 people in France each year who call on this service. The survival rate decreases by 7 to 10% for every minute that elapses between cardiac arrest and the start of cardiopulmonary resuscitation (CPR). Early CPR performed by bystanders is associated with a survival rate 2-3 times higher than CPR initiated only after emergency responders arrive on the scene. CPR assisted by SAMU-Centre 15 dispatchers (T-CPR) is a way to provide CPR to patients before emergency responders arrive on the scene and is recommended as early as possible to improve survival. According to the American Heart Association (AHA) guidelines, the timing of the initiation of the chain of survival is considered high quality if T-CPR is initiated within 90 seconds.

Studies show that recognizing a cardiac arrest (CA) over the phone is often difficult for several reasons, including communication challenges, the caller's stress, and the presence of abnormal breathing.

Emergency medical dispatchers (EMDs) receive very little training on communication strategies, particularly those needed to optimally manage stressed and sometimes difficult callers. Interventions to improve communication have proven effective among healthcare professionals. These methods included face-to-face training, blended learning programs, simulation-based teamwork exercises, and communication techniques adapted from aviation. Standardized scripting systems have been shown to improve the speed of decision-making and the dispatch of emergency response teams. These scripts depend on the quality of the information provided by the caller and the caller's ability to communicate effectively with the EMD.

The objective of this study will be to evaluate the effect of a communication training program for Centre-15 emergency medical dispatchers on calls for cardiac arrest.

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

987

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。

研究連絡先

研究連絡先のバックアップ

研究場所

      • Annecy、フランス
        • Ch Annecy-Genevois
        • コンタクト:
          • Thierry Roupioz
      • Bordeaux、フランス
        • CHU Bordeaux
        • コンタクト:
          • Xavier Combes
      • Chambéry、フランス
        • CH Métropole Savoie- Chambéry
        • コンタクト:
          • Heidi Mampe Armstrong
      • La Roche-sur-Yon、フランス
        • CH Vendée
        • コンタクト:
          • Vincent Diot
      • Lyon、フランス
        • Hospices Civils de Lyon - HEH
        • コンタクト:
          • Florent Femy
      • Nancy、フランス
        • CHRU NANCY
        • コンタクト:
          • Tahar Chouihed
      • Nantes、フランス
        • CHU Nantes
        • コンタクト:
          • Simon Ribes
      • Rennes、フランス
        • Chu Rennes
        • コンタクト:
          • Paul-Georges Reuter
      • Rouen、フランス
        • CHU Rouen
        • コンタクト:
          • Mélanie Roussel
      • Toulouse、フランス
        • CHU Toulouse
        • コンタクト:
          • Vincent Bounes

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

いいえ

説明

Inclusion Criteria:

  • Out-of-hospital cardiac arrest of presumed medical origin in an adult patient diagnosed during the phone call to the 15 emergency dispatch center

Non Inclusion Criteria:

  • Minor patients,
  • Calls initially handled by another emergency call center or a healthcare professional,
  • Calls regarding cardiac arrest for which CPR has already been initiated at the time the call is made to the 15 center,
  • Obvious or known pregnancy at the time of enrollment.
  • Persons protected under Articles L1121-6 and L1121-8 of the Public Health Code (CSP).

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:処理
  • 割り当て:ランダム化
  • 介入モデル:順次割り当て
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
介入なし:Control
Standard patient care in accordance with international recommendations. Local protocols for handling
実験的:Experimental
A multifaceted initiative combining training for SAMU Emergency medical dispatchers on the use of a standardized protocol, training on barriers to the early recognition of cardiac arrest, communication training to optimize interactions with callers, and training on handling difficult calls.
a multifaceted initiative combining training for SAMU-Centre 15 emergency medical dispatchers (EMDs) on the use of a standardized script, training on barriers to the early recognition of cardiac arrest, communication training to optimize the relationship with the caller, and training on handling difficult calls

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
The effect of a multifaceted training intervention for SAMU-Centre 15 emergency medical technicians on the proportion of patients with out-of-hospital cardiac arrest of medical origin who receive early T-RCP within 90 seconds of the call being answered,
時間枠:Baseline
The p-roportion of out-of-hospital cardiac arrests of medical origin for which T-RCP guidance is initiated within 90 seconds of the EMD answering the call will be calculated by the time to initiation of T-CPR (defined as the time elapsed between the SAMU-Centre 15 operator answering the call and the first time the operator verbally provides cardiopulmonary resuscitation instructions to the caller) The criterion will be considered met when this time is 90 seconds or less.
Baseline

二次結果の測定

結果測定
メジャーの説明
時間枠
Survival with good neurological outcome at 30 days
時間枠:30 days

Favorable neurological outcome at 30 days : Neurological outcome will be assessed by a physician using:

- the Cerebral Performance Category (CPC) scale CPC 1 : Good Cerbral Performance -> CPC 5: Brain Death

30 days
Survival with good neurological outcome at 30 days
時間枠:30 days

Favorable neurological outcome at 30 days : Neurological outcome will be assessed by a physician using:

- the modified Rankin scale Scores: 0: No Symptoms -> 5: Severe disability

30 days
Return of Spontaneous Circulation (ROSC)
時間枠:perioperatively/periprocedurally (during the CPR)
ROSC: defined by a clinical assessment of vital signs, including the presence of a palpable pulse or blood pressure
perioperatively/periprocedurally (during the CPR)
The proportion of patients admitted alive, discharged alive from the hospital, and alive at 30 days
時間枠:Day 0, day of discharge of the hospital and 30 days
Survival at hospital admission, discharge, and at 30 days
Day 0, day of discharge of the hospital and 30 days
The initial heart rate recorded
時間枠:Baseline
The initial heart rhythm recorded by a physician based on an analysis of the first heart rhythm recorded after the arrival of emergency medical personnel
Baseline
Proportion of recognized cardiac arrests
時間枠:Baseline
Percentage of calls for suspected cardiac arrest (CA) out of the total number of calls received for confirmed cardiac arrest (upon the arrival of emergency responders at the scene).
Baseline
Proportion of CAs recognized in calls for recognizable CAs
時間枠:Baseline
Percentage of calls for CAs identified relative to the number of calls received for identifiable CAs
Baseline
Proportion of CA calls receiving CPR guidance,
時間枠:Baseline
Percentage of calls receiving advice from T-RCP
Baseline
Proportion of CA calls in which the caller agrees to begin CPR for all CAs
時間枠:Baseline
Percentage of calls for CAs where the caller agrees to begin CPR for all CAs
Baseline
Time to recognize a cardiac arrest
時間枠:Baseline
Timeframe for the EMS to recognize the CA.
Baseline
Time to obtain location information
時間枠:Baseline
Time between answering the call and obtaining precise location information
Baseline
Percentage of cardiac arrests recognized within 60 seconds
時間枠:Baseline
Percentage of calls for CA recognized in less than 60 seconds, based on "recognizable" calls
Baseline
Percentage of cardiac arrests recognized within 90 seconds
時間枠:Baseline
Percentage of calls for CA recognized in less than 90 seconds, based on "recognizable" calls
Baseline
Time to begin CPR instructions
時間枠:Baseline
Timeframe for Initiating CPR instructions
Baseline
Percentage of calls where CPR instructions begin within 150 seconds
時間枠:Baseline
The proportion of out-of-hospital cardiac arrests of medical origin for which T-RCP guidance is initiated within 150 seconds of the EMD answering the call is defined by the time to initiation of T-CPR
Baseline
Quality of communication by the EMD
時間枠:Immediately after the procedure
Call quality between the EMD and the caller: The evaluation will be conducted in accordance with the recommendations published by the Haute Autorité de Santé (HAS) [85], which include guidelines for conducting interviews with callers and communication protocols. An assessment of compliance with the decision-making algorithms will also be included. The evaluation will be carried out by experts during a blinded review of the trial period.
Immediately after the procedure
Impact on service quality
時間枠:Day of inclusion
Impact analysis on Center 15 by evaluating the QS30
Day of inclusion

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • スタディディレクター:Monique Sorrentino、CHU Grenoble Alpes

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 (推定)

2026年10月1日

一次修了 (推定)

2028年8月1日

研究の完了 (推定)

2028年8月1日

試験登録日

最初に提出

2026年6月29日

QC基準を満たした最初の提出物

2026年8月17日

最初の投稿 (実際)

2026年8月20日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月20日

QC基準を満たした最後の更新が送信されました

2026年8月17日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • 38RC22.0037

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?

はい

IPD プランの説明

Study protocol will be submitted for publication. IPD will be shared with other researcher.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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