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Quick check after trauma could spot PTSD risk early

NCT ID NCT05358067

Knowledge-focused Sponsor: Centre Hospitalier Arras Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at whether a simple rating scale used by doctors right after a traumatic event can predict who will develop post-traumatic stress disorder (PTSD) later. Researchers will follow 241 adults who experienced a trauma in the last 48 hours, tracking their scores and checking for PTSD down the road. If the scale works, it could lead to a system where high-risk patients get a follow-up call to catch PTSD early and connect them to specialized care.

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 this works, doctors could use a quick rating scale to identify people at risk for PTSD right after a trauma, allowing early support and treatment.
What could go wrong
This is an observational study, not a treatment trial. The scale may not accurately predict PTSD, and results may not apply to everyone.

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 241 people

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

Started

Oct 2022

Expected to finish

Apr 2027

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

Patient who has experienced a traumatic event in the last 48 hours All patients meeting the inclusion criteria will be identified by the staff of the CUMP (medico-psychological emergency unit) either during an intervention (in the emergency department or outside) or during a psychiatric consultation at the emergencies

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: * Patient who has experienced a traumatic event in the last 48 hours; * Patient speaking French; Exclusion Criteria: * Patient participating in another clinical trial on the treatment of his psychotraumatic experience. * Person deprived of liberty (prisoners, defendants); * Persons under legal protection (protected adults: under guardianship, curatorship, etc.); * Opposition of the patient to participate in the research.

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Conditions

The condition(s) this trial relates to.

post-traumatic stress disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Post-traumatic stress disorder

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    5 sites. 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.

    Open the record ↗

  3. 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.

Contacts and locations

Locations

  • Arras General Hospital

    RECRUITING

    Arras, 62000, France

  • Arras General Hospital

    RECRUITING

    Arras, 62000, France

  • Douai General Hospital

    RECRUITING

    Douai, 59507, France

  • Lens General Hospital

    NOT_YET_RECRUITING

    Lens, 62300, France

  • Lille University Hospital

    RECRUITING

    Lille, 59000, France

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