RecruitingACTRN12612001286831

Management of patients with mild head injury in Australian Emergency Departments: The Neurotrauma Evidence Translation (NET) Trial

Testing the effectiveness of a targeted implementation intervention compared with passive dissemination on the uptake of key evidence-based recommended practices in the emergency department management of mild head injury in Australia: A cluster randomised trial


Sponsor

National Trauma Research Institute

Enrollment

34 participants

Start Date

Oct 30, 2013

Study Type

Interventional

Conditions

Summary

Head injury is a very common presentation to emergency departments (EDs). Up to 15% of patients with mild head injury experience persistent disabling problems (e.g. reduced cognitive and functional ability, heightened emotional distress, and delayed return to work or school). As the ED is the main, and often only, point of medical contact for these patients, the care they receive in the ED can impact on these patients’ outcomes. The NET-Trial is a cluster randomised trial which aims to test the effectiveness of a targeted, theory and evidence-informed implementation intervention regarding the management of adult mild head injured patients in the ED in Australia. Three recommendations from clinical practice guidelines have been selected as the focus of the study and they are 1) prospective assessment for post traumatic amnesia (PTA) using a validated tool; 2) appropriate computed tomography (CT) scanning based on risk criteria; and 3) the provision of patient information upon discharge from the ED. The 3 key evidence-based recommendations have been decided after a systematic review of the evidence and available clinical guidelines, and consultation with the ED community. EDs will be randomised to receive either the intervention or to a control group who will have access to the clinical practice guideline alone. The control group will be offered to receive the intervention component of the study following data collection. In addition, EDs will be invited to participate in the “NET-Plus” trial that also includes patient outcomes to investigate whether improved management as a result of our intervention is translated into improved patient outcomes.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This study is testing a targeted education and support program for emergency department staff to improve how they assess and treat patients with mild head injuries. Up to 15% of people with a mild head injury have long-lasting problems such as memory issues, emotional distress, or difficulty returning to work. Researchers want to see whether following evidence-based guidelines more consistently leads to better patient outcomes. You may be eligible if: - You are 18 years or older - You have come to an emergency department within 24 hours of a head injury - Your Glasgow Coma Score (a measure of consciousness) was 14 or 15 on arrival You may NOT be eligible if: - You have a penetrating head injury - Your brain injury was caused by a stroke or other non-traumatic event - You are unable to answer follow-up questions (for example, if you do not speak English) Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Emergency departments (EDs) randomised to the intervention arm will receive a targeted, theory and evidence-informed implementation intervention designed to increase the uptake of key evidence-based r

Emergency departments (EDs) randomised to the intervention arm will receive a targeted, theory and evidence-informed implementation intervention designed to increase the uptake of key evidence-based recommended practices in the management of mild head injured patients. The intervention will involve local stakeholder meetings, identification of nursing and medical clinical opinion leaders in each site; a train-the-trainer day; materials to increase the visibility of tools; and a non-specific reminder to optimise data collection and standardised education and interactive workshops delivered by the clinical leaders over a 3 month period of time.


Locations(1)

ACT,NSW,NT,QLD,SA,TAS,WA,VIC, Australia

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ACTRN12612001286831


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