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Sensory sensitivity may signal PTSD risk after combat

NCT ID NCT05967962

Knowledge-focused Sponsor: Tel Aviv University 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether people with sensory modulation problems (like being overly sensitive to sounds or touch) are more likely to develop PTSD after a traumatic event. Researchers showed 248 healthy adults a stressful film and tracked their memories, pain sensitivity, and stress hormones. The goal was to understand how sensory issues might make someone more vulnerable to PTSD.

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

248 people

The number who actually took part.

Started

May 2023

Finished

Feb 2025

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 to 28 years

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: * Intact or corrected vision * Proficiency in Hebrew * Exclusion Criteria: * Neurological disorders * Psychiatric disorders * Neurodevelopmental disorders * Substance use disorder * Chronic pain * Regular intake of medications. * Cultural and societal backgrounds that might bias participant reaction to study protocol (i.e., nationality)

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Conditions

The condition(s) this trial relates to.

injury post-traumatic stress disorder prevention target

As listed by the trial registrant

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

Posttraumatic stress disorder Sensory processing disorder

Contacts and locations

Locations

  • Dr. Tami Bar-Shalita

    Tel Aviv, Israel

More trials for these conditions

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