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Can a simple health watch prevent trauma after a scary event?

NCT ID NCT06366191

Prevention Sponsor: Centre Hospitalier Universitaire de la Réunion Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 24, 2026 · Last updated Sep 15, 2026 · Updated 3 times

Summary

This pilot study tests whether a special health watch that monitors stress and dissociative symptoms can help prevent psychological trauma after a traumatic event. About 40 people who have experienced a potentially traumatic event will either receive standard care alone or standard care plus this watch. The main goal is to see if people find the approach acceptable and stick with it.

What this could mean

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

Active substance
prevention algorithm (health watch with stress and dissociative symptom monitoring)
What this could lead to
If it works, this could point toward a simple way to prevent post-traumatic stress disorder after a traumatic event.
What could go wrong
This is a very small pilot study with only 40 participants, so results may not apply broadly. The main goal is to see if people accept the approach, not yet to prove it prevents trauma.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 40 people

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

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Nov 2026

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.

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: * Person who the vital prognosis has or could have been committed or having felt a threat to his physical and/or psychological integrity * After a potentially traumatic event dating from a minimum of 72 hours to a maximum of 1 week * for which the CUMP or the psychotrauma regulation platform has been requested * having lived or being a direct witness of the event * knowing how to read and write * affiliate or beneficiary of a social security scheme * having signed a consent Non-inclusion Criteria: * guardianship or curatorship * unable to receive phone calls * unable to go to a place for consultation

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Conditions

The condition(s) this trial relates to.

Psychological Trauma

As listed by the trial registrant

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

Psychological trauma

How to take part

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

  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.

    Open the record ↗

  2. 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.

More trials for these conditions

Other studies related to the condition(s) this trial covers.