What really matters in the ER? study seeks to measure the unseen value of healthcare workers

NCT ID NCT07686666

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

About 1,350 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 2030

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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

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  1. 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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  2. A doctor treating you

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