Scientists ask trauma patients: what scares you most after injury?

NCT ID NCT07811830

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.
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
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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 Results may not be published yet.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

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Status unknown
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First seen Sep 10, 2026 · Last updated Sep 11, 2026 · Updated 1 time

Summary

Researchers want to understand what concerns trauma patients most right after an injury. The study enrolls 300 adults who arrive at the emergency department with an acute injury and are stable enough to take part. Participants fill out a questionnaire about their stress, pain, and worries, including fears about surgery, family, children, work, and money. Hospitalized patients answer a second questionnaire about a day later.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
a questionnaire and physical exam
What this could lead to
If researchers learn which concerns weigh most on trauma patients, emergency teams could tailor information and support to address those worries sooner.
What could go wrong
This is an observational survey with no treatment, so it cannot prove that addressing any specific concern improves outcomes. Patients in severe distress may not complete questionnaires, which could skew the picture.

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 300 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Aug 2028

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 consists of adult patients aged 18 years or older presenting to the Emergency Department with an acute traumatic injury and classified as triage category 3, 4, or 5. Eligible participants must be clinically stable after the initial medical assessment, able to understand the study information and questionnaires, and capable of providing written informed consent. Patients who require hospitalization will additionally complete a follow-up questionnaire approximately 24 hours after admission.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: 1. Age 18 years or older. 2. Presentation to the Emergency Department because of an acute traumatic injury. 3. Triage category 3, 4, or 5. 4. Clinical stability after the initial assessment. 5. Ability to understand the study information and the questionnaire. 6. Ability to provide written informed consent Exclusion Criteria: 1. Triage category 1 or 2 (an acutely life-threatening condition or an immediate need for emergency medical or surgical intervention; hemodynamic or respiratory instability). 2. Severe impairment of consciousness, disorientation, or inability to cooperate. 3. Inability to provide informed consent; cognitive impairment or a language barrier preventing comprehension of the questions. 4. Severe alcohol or drug intoxication preventing valid completion of the questionnaire. 5. A situation in which completion of the questionnaire is inappropriate for medical, ethical, or organizational reasons.

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Conditions

The condition(s) this trial relates to.

Emergencies injury

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 places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

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Contacts and locations

Locations

  • OŽB Požega

    Požega, 34000, Croatia

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