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Peers Vs Professionals in Basic Life Support Training

2018年4月27日 更新者:Damascus University

Peers Versus Professional Training of Basic Life Support in Syria: a Randomized Controlled Trial

An Evaluation of Peer-led basic life support training course compared with professional-led course in a limited resource environment; A randomized controlled trial

調査の概要

詳細な説明

Peer training has been identified as a useful tool for delivering undergraduate training in basic life support (BLS) which is fundamental as an initial response in cases of emergency.

This study aimed to (1) Evaluate the efficacy of peer-led model in basic life support training among medical students in their first three years of study, compared to professional-led training and (2) To assess the efficacy of the course program and students' satisfaction of peer-led training.

A randomized controlled trial with blinded assessors will be conducted on 72 medical students from the pre-clinical years (1st to 3rd years in Syria) at Syrian Private University. Students will be randomly assigned to peer-led or to professional-led training group for one-day-course of basic life support skills.

Analysis will be done on students who underwent checklist based assessment using objective structured clinical examination design (OSCE) (practical assessment of BLS skills) and answered BLS knowledge checkpoint-questionnaire.

研究の種類

介入

入学 (実際)

72

段階

  • 適用できない

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

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Medical student from 1st, 2nd and third year at Syrian Private University.
  • Sign the consent form.

Exclusion Criteria:

  • presence of any health problems preventing students from doing physical exercise.
  • any serious acute or chronic illness (infectious, psychological, physical).
  • scheduling conflict between the date of the BLS course and other faculty's classes or exams.
  • missing the course or the assessment for any reason.
  • refusing to sign the consent and having any prior experience in BLS skills (previously trained on BLS).

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:並列代入
  • 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
実験的:Peers' group

36 Medical students are allocated randomly to Peers' group where they are trained on BLS skills by senior students.

Four students from the latest three years of study in medical schools in Syria (4th, 5th, and 6th) are randomly selected and enrolled to be instructors for basic life support training course to transfer the resuscitation skills to medical students from pre-clinical years.

A course design was made to be consistent with ERC guidelines with local modifications made by emergency professionals in duration, instructor-to-trainee ratio, course materials, methods to deliver these materials theoretically, and the type of the manikin used to practice CPR. One-day-course consisting of 75, 20, 20, 20 minutes for theoretical BLS, chocking, recovery position, the practical representation of BLS scenario respectively followed by 40-minute practical training on BLS skills for each subgroup. Both arms of the study follow the same timeline and no extra time is given to any group.

Same manikins were used for the training and the assessment. On the day of the experiment students in each arm are divided into 4 subgroups of maximum 9 students, each led by two trainers of BLS skills with a maximum ratio of 2 instructors to 9 students per group.

実験的:Professionals' group
36 students are allocated randomly to professionals' group where they are trained on BLS skills by professional trainers in emergency. Four professionals (2 emergency doctors, cardiologist and anesthesiologist) are leading training to the control group to deliver the basic life support training course with the same duration and content as the intervention group.

A course design was made to be consistent with ERC guidelines with local modifications made by emergency professionals in duration, instructor-to-trainee ratio, course materials, methods to deliver these materials theoretically, and the type of the manikin used to practice CPR. One-day-course consisting of 75, 20, 20, 20 minutes for theoretical BLS, chocking, recovery position, the practical representation of BLS scenario respectively followed by 40-minute practical training on BLS skills for each subgroup. Both arms of the study follow the same timeline and no extra time is given to any group.

Same manikins were used for the training and the assessment. On the day of the experiment students in each arm are divided into 4 subgroups of maximum 9 students, each led by two trainers of BLS skills with a maximum ratio of 2 instructors to 9 students per group.

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
BLS practical skills
時間枠:Training and assessment were held at the same day of the experiment for both groups, 1) within 24 hours of providing the bls training course.
A practical simulated scenario assessment using a checklist based evaluation in objective structured clinical examination (OSCE) design. The checklist is constructed in accordance to European resuscitation council (ERC) guideline. Students should perform each point correctly to pass the assessment (1- Safe approach, 2- call for help, 3- opening airway, 4-checking cardiopulmonary situation, 5- call ambulance, 6- CPR with effective depth, 7-rate and 8-position, 9-rescue breaths).
Training and assessment were held at the same day of the experiment for both groups, 1) within 24 hours of providing the bls training course.

二次結果の測定

結果測定
メジャーの説明
時間枠
BLS knowledge questionnaire
時間枠:Training and assessment were held at the same day of the experiment for both groups. 1) within 24 hours of providing the bls training course.
a 20-item questionnaire with 3 checkpoints per item (60-point-scale) derived from ERC materials after testing the applicability of the questionnaire by a pilot study.
Training and assessment were held at the same day of the experiment for both groups. 1) within 24 hours of providing the bls training course.
Students' evaluation of BLS course survey
時間枠:Training and assessment were held at the same day of the experiment for both groups. 1) within 24 hours of providing the bls training course.
Students' reported outcomes using American Heart Association (AHA) survey of BLS course evaluation. This survey aims to investigate students' satisfaction and their opinions about the course.
Training and assessment were held at the same day of the experiment for both groups. 1) within 24 hours of providing the bls training course.

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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)

2016年3月1日

一次修了 (実際)

2016年5月1日

研究の完了 (実際)

2016年10月1日

試験登録日

最初に提出

2018年4月12日

QC基準を満たした最初の提出物

2018年4月27日

最初の投稿 (実際)

2018年4月30日

学習記録の更新

投稿された最後の更新 (実際)

2018年5月1日

QC基準を満たした最後の更新が送信されました

2018年4月27日

最終確認日

2018年4月1日

詳しくは

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未定

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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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