What really matters in the ER? study seeks to measure the unseen value of healthcare workers
NCT ID NCT07686666
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This study investigates the experiences of healthcare professionals, patients, and families in high-acuity hospital settings like emergency rooms and intensive care units. Researchers aim to understand less visible contributions such as teaching, coordination, and emotional support, as well as challenges like burnout and moral injury. By gathering insights through questionnaires and interviews, the study hopes to identify areas for future improvements in hospital practices and policies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could identify key areas for improving support and reducing burnout among healthcare workers in high-stress hospital settings.
- What could go wrong
- This is an early exploratory study, not a clinical trial of a treatment. Findings may not lead to direct changes and are based on subjective experiences.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 1,350 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population includes adults aged 18 years or older with work, care, caregiving, or system-related experience in high-acuity medical care settings. Participants may include healthcare professionals working in hospital-based emergency, trauma, intensive care, respiratory care, and related clinical areas; patients who have received care in these settings; important family members or main caregivers; and public-sector or emergency response personnel involved in emergency care, rescue, health, or social service systems.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 18 years or older who are able to understand the study information and provide informed consent or agreement to participate. * Healthcare professionals working in hospital-based high-acuity clinical areas, such as emergency departments, trauma and critical care, intensive care units, respiratory care units, and related settings. Eligible participants may include physicians, nurses, allied health professionals, case managers, registry or data management personnel, and administrative staff involved in these areas. * Patients who have received care in high-acuity medical care settings. * Important family members or main caregivers who have accompanied, cared for, or supported decision-making for patients in high-acuity medical care settings. * Public-sector or emergency response personnel involved in emergency care, rescue, health, or social service systems related to high-acuity medical care. For the first phase, healthcare professionals may be invited to complete questionnaires and/or participate in qualitative interviews. Patients, important family caregivers, and other relevant stakeholders may be invited to participate in qualitative interviews. For the second phase, eligible stakeholder groups may be invited to complete an anonymous online survey. Exclusion Criteria: * Individuals who decline to participate after receiving the study explanation. * Individuals who do not meet the inclusion criteria. * Individuals who are unable to understand the study information or complete the study procedures.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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