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PTSD patients misjudge future feelings, study finds

NCT ID NCT05268965

Knowledge-focused Sponsor: University Hospital, Lille Source: ClinicalTrials.gov ↗

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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 Results may not be published yet.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)

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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
This status has not been confirmed recently, so it may be out of date.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 how people with post-traumatic stress disorder (PTSD) predict their emotional reactions to future events. Researchers compared 97 participants with and without PTSD to see if those with PTSD tend to expect more intense negative emotions than they actually experience. The goal was to better understand the thinking patterns linked 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.

Participants

97 people

The number who actually took part.

Started

Feb 2022

Finished

Nov 2023

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

subjects suffering from post-traumatic stress disorder (PTSD)

Ages

18 to 60 years

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: * Understanding and being able to express themselves in French * Understanding of informed consent and signature of the study participation form * Giving informed, dated and signed consent * Benefiting from health insurance coverage * Normal or corrected visual and auditory acuity to achieve normality * Group 1 : DSM-5 PTSD criteria, assessed using CAPS and PTSD Checklist for DSM-5 (PCL-5, Weathers \& al., 2013) * Group 2: PTSD Criteria A only Exclusion Criteria: Refusal of participation after clear and fair information on the study. * Visual or auditory sensory disability to participate in the study. * Personal history of neurological disease or current neurological disease. * Personal history of current psychiatric disorder or psychiatric disorder (excluding PTSD in patients in the experimental group), assessed via the MINI. * Pregnant or breastfeeding women * Consumption of toxic substances other than tobacco and alcohol. * Minors or adults under guardianship, under judicial protection, persons deprived of liberty. * Groups 2 and 3: personal history of psychiatric disorder or current psychiatric disorder and taking psychotropic drugs * Group 1: personal history of psychiatric disorders or current psychiatric disorders other than anxiety, depressive, trauma and stress-related disorders and treatment with psychotropic drugs not stabilized

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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

Contacts and locations

Locations

  • Usn Fontan - Linquette Chu Lille

    Lille, France

More trials for these conditions

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