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Facial Emotion Recognition in Patients With Euthymic Bipolar Disorder I and II (REF-BIP)

C

Centre Hospitalier Universitaire, Amiens

Status

Completed

Conditions

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

Treatments

Other: Facial emotion recognition test

Study type

Interventional

Funder types

Other

Identifiers

NCT05922956
PI2020_843_0009

Details and patient eligibility

About

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.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

10 participants in 3 patient groups

patients with bipolar disorder 1
Experimental group
Treatment:
Other: Facial emotion recognition test
patients with bipolar disorder 2
Experimental group
Treatment:
Other: Facial emotion recognition test
healthy controls
Active Comparator group
Treatment:
Other: Facial emotion recognition test

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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