Can the Brain's Information-Integration process explain Anorexia's grip?
NCT ID NCT02381639
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Researchers at Nantes University Hospital are studying central coherence, the brain's ability to pull complex information into a coherent whole, in women with restrictive anorexia nervosa. The study compares patients in the active phase of the illness with healthy volunteers. All participants complete a 90-minute session of cognitive tests and self-assessment questionnaires. The goal is to understand whether differences in central coherence relate to the disorder and could inform future cognitive remediation therapies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a 90-minute interview combining cognitive tests and self-assessment questionnaires
- What this could lead to
- If researchers find a link between central coherence and anorexia nervosa, it could point toward cognitive remediation therapies that target this thinking process.
- What could go wrong
- This is an observational study with no treatment, so it cannot prove that central coherence problems cause or maintain anorexia. The findings may not apply to men or to people outside this single hospital in Nantes.
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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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122 people
The number who actually took part.
- Started
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Jun 2015
- Finished
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Aug 2017
- Lead sponsor
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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
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15 years and older
- Sex
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Female participants only
- 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.
Inclusion Criteria: * For the patients : * Woman. * Aged of more than 15 years and 3 months. * Followed in the addiction service of the University Hospital of Nantes (consultations and / or hospitalizations) for Restrictive Anorexia Nervosa (according to the diagnostic criteria of DSM-IV-TR). * French language mastered. * Having signed the consent if major and if not the legal representatives have signed the consent (for minors). * For the volunteers : * Women. * Aged of more than 15 years and 3 months. * French language mastered. * Having signed the consent if major and if not the legal representatives have signed the consent (for minors). Exclusion Criteria: * For the patients : * Man * Age under 15 years and 3 months old * Current Renutrition by nasogastric tube * Personal history of: * Head injury, neurodegenerative diseases, epilepsy unbalanced, unbalanced endocrine disorder, mental retardation * Support for current or past cognitive remediation * Opposition of the patient and / or his legal representatives if minor * Subject under legal guardianship * Current participation or in the past to pharmacological research protocol (time since the end of their participation in the protocol less than one year) * French language not mastered * For the volunteers : * Man * Age under 15 years and 3 months old * Current Renutrition by nasogastric tube * Personal history of: * Eating disorders * Head injury, neurodegenerative diseases, epilepsy unbalanced, unbalanced endocrine disorder, mental retardation * Support for current or past cognitive remediation * Opposition of the volunteer and / or his legal representatives if minor * Subject under legal guardianship * Current participation or in the past to pharmacological research protocol (time since the end of their participation in the protocol less than one year) * French language not mastered
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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.
Contacts and locations
Locations
-
CHU de Nantes, Service d'Addictologie
Nantes, France
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