Insomnia may cloud your ability to read emotions, study suggests
NCT ID NCT06251258
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares how people with chronic insomnia and healthy controls recognize facial emotions. Using eye-tracking, researchers will look for subtle differences in attention and emotional processing. The goal is to better understand social challenges linked to insomnia and inform future therapies.
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 improve understanding of social difficulties in insomnia and guide targeted cognitive-behavioral therapies.
- What could go wrong
- This is an observational study with no treatment being tested. Results may not lead to immediate clinical changes.
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
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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
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About 128 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
Pre-inclusion criteria * Age between 18 and 65 * Signed consent to participate in the study * Person affiliated to or benefiting from a social security scheme * For insomnia group: known insomnia (patient treated for insomnia) Inclusion criteria: * Insomnia group: ISI \>14 (between 15 and 28 = clinical insomnia) * Control group: ISI \< 8 (between 0 and 7 = no insomnia) Non-pre-inclusion criteria * Known psychiatric disorders (Characterized depressive episode, Bipolar disorder, Schizophrenia and other delusional disorders, Specified anxiety disorder (social anxiety, generalized anxiety disorder), Obsessive-compulsive disorder (OCD), Eating disorders, Neurodevelopmental disorders (ASD, ADHD), Active addictive disorders (excluding tobacco), ...) * Taking antidepressant, neuroleptic or thymoregulator medication * Taking a benzodiazepine with a long half-life (\>12 hours) * Condition requiring hospitalization in the month preceding the study * Known sequelae or progressive neurological disease * Known significant ophthalmological condition * Pregnancy or breast-feeding * Person deprived of liberty by judicial or administrative decision * Person subject to a legal protection measure * Person under psychiatric care without consent * For control group: no known insomnia Non-inclusion criteria : \- Psychiatric disorders identified during psychiatric interview
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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CHU Angers
RECRUITINGAngers, 49033, France
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