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Facial Emotion Recognition in Patients With Euthymic Bipolar Disorder I and II

Facial Emotion Recognition in Patients With Euthymic Bipolar Disorder I and II

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05922956
Acronym
REF-BIP
Enrollment
10
Registered
2023-06-28
Start date
2020-04-01
Completion date
2023-07-01
Last updated
2025-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder I and II, Facial Affect, Facial Emotion Recognition, Social Cognition

Keywords

social cognition, facial emotion recognition, facial affect, bipolar disorder I and II

Brief summary

The facial emotion recognition is a basic social skill for successful social interactions. Several meta-analyses and recent studies found impairments of the perception of facial emotions in patients with euthymic bipolar disorder. Few studies compared recognition of facial emotions impairments during euthymia in patients with bipolar disorder type 1 and 2. These studies included low population samples (N\<60). There were discrepancies in results of these studies. Szanto suggested that facial emotion recognition impairments were correlated with suicidal risk and social isolation. These impairments should be taking into account regarding psycho-social treatments in patients with bipolar disorder. This study aims to evaluate facial emotion recognition in patients with bipolar I and II disorders compared to healthy controls, using the facial emotion recognition test (TREF). The objective of the present study is to compare TREF scores in a group of patients with bipolar 1, a group of patients with bipolar 2 disorder and a group with healthy controls. In addition, the investigators will investigate the relationships between TREF scores and levels of self-esteem and mental well-being.

Interventions

Facial emotion recognition test (TREF), questionnaires including self-administered questionnaires

Sponsors

Centre Hospitalier le Vinatier
CollaboratorUNKNOWN
Pôle Ressource Évaluation et Réhabilitation Psycho-sociale, EPSM de l'Oise
CollaboratorUNKNOWN
Centre de santé mentale MGEN
CollaboratorUNKNOWN
Centre Hospitalier Philippe Pinel, Amiens
CollaboratorUNKNOWN
Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patient group : * Male or female patients, between 18 and 60 years old * Diagnosis of Bipolar Disorder I or Bipolar Disorder II according to DSM-IV criteria, using the French version of the Mini-International Neuropsychiatric Interview (MINI) * Strictly euthymic defined by Hamilton Depression Rating Scale (17 items) ≤ 5 and Young Mania Rating Scale ≤ 5 for at least two months. * Native French speakers * Affiliated to the French social security system * Giving their written informed consent Control group : * Male or female control subjects, aged between 18 and 60 years old, assessed using TREF * Native French speakers * Giving their written informed consent

Exclusion criteria

* Patient group : * History of mental retardation assessed by the French version of the National Adult Reading Test * Neurological illness or any clinical condition that could affect cognitive performance (history of head injury with loss of consciousness lasting more than 5 minutes multiple sclerosis, stroke etc.) * Electroconvulsive therapy within the last 6 months * Alcohol and Drug dependence (except tobacco and caffeine) according to DSM-IV criteria using the French version of the Mini-International Neuropsychiatric Interview (MINI). * Learning disability or difficulty with fluent use of the French language * Patient with mandatory care * Long-Term use of non-psychotropic medication with psychotropic effects (opiates, Baclofen) Control group : * History of mental retardation estimated by the French version of the National Adult Reading Test * Neurological illness or any clinical condition that could affect cognitive performance (history of head injury with loss of consciousness lasting more than 5 minutes multiple sclerosis, stroke etc.) * Current Mood disorder/ Lifetime Psychotic Disorder according to DSM-IV criteria using the French version of the Mini-International Neuropsychiatric Interview (MINI) * Neither history of psychotic or affective disorders in a first-degree family member * Alcohol and Drug dependence (except tobacco and caffeine) according to DSM-IV criteria using the French version of the Mini-International Neuropsychiatric Interview (MINI) * Learning disability or difficulty with fluent use of the French language * Long-Term use of non-psychotropic drugs with psychotropic effects (opiates, Baclofen) and psychotropic drugs

Design outcomes

Primary

MeasureTime frameDescription
variation of TREF scores in tree groups of subjects16 monthsTREF scores in tree groups of subjects (group of patients with bipolar disorder 1, group of patients with bipolar disorder 2 and group of healthy controls.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026