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Stroke's hidden toll: brain scans reveal emotion perception changes

NCT ID NCT05595005

Knowledge-focused Sponsor: University Hospital, Lille 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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at how stroke changes the brain's ability to recognize emotions like fear and happiness. Researchers used MRI and EEG to compare stroke patients with healthy volunteers. The study was stopped early and only included 2 participants, so findings are very limited.

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 successful, this research could help develop better therapies for emotional perception problems after stroke.
What could go wrong
The study was terminated early with only 2 participants, so results are very limited and may not be reliable. It was a small, early-stage observation.

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

2 people

The number who actually took part.

Started

Feb 2024

Finished

Feb 2026

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 group: 40 subjects Healthy control group: 40 subject

Ages

18 to 80 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: Stroke group: * Man or Woman * Age 18-80y * Unique stroke, ischemic or hemorrhagic * at the chronic phase (\< 6 months) * Written informed consent * subject having a social insurance * Subject who consent to complete all the study's experiments Healthy controls group: * Man or Woman * Age 18-80y * No history of neurological or psychiatric disease. Exclusion Criteria: Stroke group * Subject who is unable to consent (due to dementia, severe aphasia, psychiatric disorder...) * History of other neurologic disorders * Significant le vel of depression or anxiety, assessed by the STAI and the BDI questionnaires * Non corrected visual loss * Subjects suffering from visual neglect (assessed by the Bells Test and a bisection test (20mm) * contra-indications to MRI * pregnant or breastfeeding woman * Women of childbearing age without effective contraception Healthy controls group * Subject who is unable to consent (due to dementia, severe aphasia, psychiatric disorder...) * History of neurologic disorders * Significant level of depression or anxiety, assessed by the STAI and the BDI questionnaires * Non-corrected visual loss * contra-indications to MRI * pregnant or breastfeeding woman * Women of childbearing age without effective contraception

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Conditions

The condition(s) this trial relates to.

stroke disorder

As listed by the trial registrant

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

Emotions Stroke Stroke sequelae

Contacts and locations

Locations

  • Hôpital Swynghedauw

    Lille, 59037, France

More trials for these conditions

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