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Набор скоро начнётся NCT07314437

5 Minute 'HOT' Trauma CT Rates Of Detection Study

Без фазы С лечением Trauma (Including Fractures) Trauma Abdomen Trauma Blunt Trauma Centers

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: Education.
Кому может быть актуально
Состояния в реестре: Trauma (Including Fractures), Trauma Abdomen, Trauma Blunt, Trauma Centers. 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
Великобритания
Следующий шаг
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Официальное название

Randomised Trial (With Integrated Pilot) Evaluating Whether a Standardised Approach, Educational Package (Including Checklist) Improve Recognition of Major Life-threatening Injuries in the Hot Reporting of Trauma Scans

Обзор

Many injured patients receive urgent CT imaging to identify major injury. CT imaging of trauma patients is often time critical and the accurate detection of life-threatening findings on this CT is essential. Often following a scan a radiologist is not immediately available to review the imaging, however other members of the trauma team have access to the imaging and may be in a position to provide a "hot" report. In this study we aim to demonstrate if an educational intervention with a checklist improves accuracy of the hot report.

Подробное описание

This is a randomised controlled trial to evaluate whether a standardised approach, educational package (with checklist) may improve recognition of major life-threatening injuries in the hot reporting of trauma scans. A pilot study with 20 participants allocated to the two groups on 1:1 ratio which will receive the education package, will inform feasibility of the larger study.

The larger study will recruit 300 participants, 100 on each group on 1:1:1 ratio, to evaluate the primary objective.

Participants will be clinicians who volunteer to participate in an online educational package. Participant data will be collected by the online platform under a unique identifier. Results will then be extracted from the platform and then associated with the demographic data on the trust system.

Following application of inclusion and exclusion criteria, participants will be allocated into one of three groups, and assigned a participant number. The test data set will consist of cases that have been pseudo anonymised with the key stored on trust systems.

Вмешательства

  • Другое Education
    The three groups will report 2 image banks of 15 CT images each. Image bank A will contain 15 CT images each with a brief history including the mechanism of injury. Image bank B will contain 10 new CT images and 5 CT images contained within image bank A, but with an altered but compatible mechanism of injury. Group 1 will report image bank A, receive the educational intervention and then report image bank B with the checklist. Group 2 will report image bank B, receive the educational interventi

Первичные конечные точки

  • Rates of detection and error of a hot CT report. [Срок оценки: 1 year]

Критерии участия

Критерии включения

  • Medical professionals involved in trauma image review.
  • This includes clinicians who are emergency department doctors, radiologists and other specialties.
  • Non-radiologist clinicians will be participating completing the hot reports, radiologists will be evaluating their submissions and assessing their accuracy.

Критерии исключения

  • Unable to review CT imaging due to lack of previous experience or disability that prevents them from doing so.
  • Under 18 years old.
  • Not a medical professional or clinician.

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Факторный дизайн
Маскирование
Простое слепое
Основная цель
Диагностика

Центры проведения

Великобритания · 1 центр
  • University Hospitals Plymouth — Plymouth

Идентификаторы

NCT: NCT07314437 · 25/RAD/176 · 361877 · 70122

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗