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Идёт набор NCT06867653

Different Re-training Durations in BLS Training Among Non-Professionals

Без фазы С лечением Education Curriculum

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Retraining.
Кому может быть актуально
Состояния в реестре: Education Curriculum. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Тайвань
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Different Re-training Durations in Basic Life Support Training Among Non-Professionals: A Three-Arm Randomized Controlled Trial

Обзор

Previous studies on compression-only CPR and AED training for the general public have primarily focused on the optimal retraining interval. However, the impact of different retraining durations remains unclear. This study explores how varying practice durations in Basic Life Support (BLS) training affect BLS performance among non-professionals.

Подробное описание

In this study, participants first underwent compression-only CPR and AED training. Before training, they completed a questionnaire on their perspectives on BLS retraining and basic demographic information. Knowledge tests, skill assessments, and attitude and confidence questionnaires were conducted both before and after training. During the skill assessment, two cameras recorded the process from different angles: one positioned from the feet towards the head of the manikin and the other from the left chest towards the right chest. Instructors, blinded to group allocation, later reviewed the recordings and assessed participants' performance using an evaluation form. Additionally, chest compressions were recorded using a computerized manikin (SkillReporter Resusci Anne®, Laerdal, Stavanger, Norway).

Participants were then randomly assigned to one of three groups based on different retraining durations:

1. 45-minute retraining sessions 2. 60-minute retraining sessions 3. 75-minute retraining sessions

All three groups underwent skill assessments and knowledge tests every three months before their respective retraining sessions. The retraining skill assessments followed the same procedure as the initial training. Each retraining session began with a 15-minute comprehensive review, followed by hands-on practice. Each participant practiced for approximately five minutes per cycle, which included two minutes of chest compressions, one minute of AED application, one minute of feedback, and one minute for role-switching. Based on this structure, participants in the 45-minute group completed two practice cycles, those in the 60-minute group completed three cycles, and those in the 75-minute group completed four cycles.

Both the initial training and retraining followed the American Heart Association (AHA) Heartsaver® CPR+AED course guidelines, with a participant-to-manikin ratio of 3:1 and a maximum of six participants per instructor. One year after the initial training, before the final skill assessment, participants completed the knowledge test and the attitude and confidence questionnaire. After the final skill assessment, they completed the CPR retraining perspectives questionnaire.

Вмешательства

  • Другое Retraining
    Each retraining session begins with a 15-minute comprehensive review, followed by hands-on practice

Первичные конечные точки

  • Average compression rate [Срок оценки: one year after the initial training]
Вторичные конечные точки (9)
  • Average compression depth [Срок оценки: 3, 6, 9 and 12 months after the initial training]
  • Average compression rate [Срок оценки: 3 month, 6 months and 9 months after initial training]
  • Chest recoil [Срок оценки: 3, 6, 9 and 12 months after the initial training]
  • Flow time [Срок оценки: 3, 6, 9 and 12 months after the initial training]
  • Correct hand placement [Срок оценки: 3, 6, 9 and 12 months after the initial training]
  • Pass rate [Срок оценки: 3, 6, 9 and 12 months after the initial training]
  • Passing rates for each item [Срок оценки: 3, 6, 9 and 12 months after the initial training]
  • Attitude [Срок оценки: one year after the initial training]
  • Confidence [Срок оценки: one year after the initial training]

Критерии участия

Критерии включения

  • Age >=18 years old

Критерии исключения

  • Subjects whose physical condition is unsuitable for the CPR training, such as those unable to squat, extend their arms fully, or individuals who are blind or deaf.
  • Healthcare professionals and students majoring in healthcare-related fields.
  • Individuals unwilling to sign the informed consent form

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Другое

Центры проведения

Тайвань · 1 центр
  • National Taiwan University Hospital — Taipei

Идентификаторы

NCT: NCT06867653 · 202007002RINB

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗