5 Minute 'HOT' Trauma CT Rates Of Detection Study

NCT ID: NCT07314437

Last Updated: 2026-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-30

Study Completion Date

2027-02-28

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Trauma (Including Fractures) Trauma Abdomen Trauma Blunt Trauma Centers

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

The primary analysis will be comparative between the pickup rate between the first and second imaging set within groups 1 and 2. Group 3 will act a control group to determine the effect of repetition on skill development rather than the education package. Subgroup analysis of clinicians by demographics including trauma experience will be performed.
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

SINGLE

Participants
Each Group will not be aware of the intervention or education or content the other Group receives.

Study Groups

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Group 3 Control Group

No intervention. Control Group.

Group Type NO_INTERVENTION

No interventions assigned to this group

Group 1 Intervention Group A Images

Group 1 will report image bank A, receive the educational intervention and then report image bank B with the checklist.

Group Type EXPERIMENTAL

Education

Intervention Type OTHER

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 intervention and then report image bank A. Group 3 will report image bank A and B without any intervention.

Group 2 Intervention Group B Images

Group 2 will report image bank B, receive the educational intervention and then report image bank A.

Group Type EXPERIMENTAL

Education

Intervention Type OTHER

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 intervention and then report image bank A. Group 3 will report image bank A and B without any intervention.

Interventions

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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 intervention and then report image bank A. Group 3 will report image bank A and B without any intervention.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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.

Exclusion Criteria

* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital Plymouth NHS Trust

OTHER

Sponsor Role lead

Responsible Party

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Paul Jenkins

Consultant Interventional Radiologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University Hospitals Plymouth

Plymouth, Devon, United Kingdom

Site Status

Countries

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United Kingdom

Central Contacts

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Paul Jenkins, BMBS, BSc (Hons), FRCR, EBIR

Role: CONTACT

+441752430838

Facility Contacts

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Paul Jenkins, BMBS, BSc (Hons), FRCR, EBIR

Role: primary

+441752430838 ext. 30838

Gabriela Di Scenza, MBBS, BA (Hons), PGCert

Role: backup

+447973177122

Other Identifiers

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361877

Identifier Type: OTHER

Identifier Source: secondary_id

70122

Identifier Type: OTHER

Identifier Source: secondary_id

25/RAD/176

Identifier Type: -

Identifier Source: org_study_id

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