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Study of Intra- and Interpersonal Multimodal Synchronizations in a Social Interaction in Individuals with a Diagnosis of Schizophrenia.

Not Applicable
Recruiting
Conditions
Schizophrenia
Interventions
Behavioral: Social interaction
Registration Number
NCT06484387
Lead Sponsor
University Hospital, Montpellier
Brief Summary

The aim of this study is to precisely identify deficits in intra- and interpersonal multimodal synchronizations during social interaction in individuals with schizophrenia (ISZ). During a social interaction, individuals use both visual and auditory channels to construct their discourse. The auditory channel encompasses the semantics and prosody of the speech, while the visual channel describes the entirety of non-verbal gestures (e.g., facial expressions, body movements). Prosody and non-verbal gestures are essential elements for the speaker. By accompanying speech, they contribute to the planning and conceptualization of the utterance and enhance its communicative power. For the listener, prosody and non-verbal gestures are also used to provide sensory feedback to the speaker.

Several studies have shown the existence of intrapersonal and interpersonal synchronizations of prosody and non-verbal gestures during interaction. These synchronizations are associated with numerous social benefits (e.g., increased mutual appreciation and quality of interaction). However, certain mental disorders, such as schizophrenia, exhibit deficits in non-verbal behaviors that can impair these synchronizations and the associated social benefits. We hypothetized that interaction with individuals with a daignosis of schizophrenia will be associated with deficits in intra and interpersonal synchronization.

Detailed Description

This study includes a pre-inclusion interview followed by a visit to the university hospital (CHU) lasting about 2 hours (including a break). During the visit, the patient participates in an experimental protocol consisting of two parts. In the first part, the patient will be paired with an interaction partner, and the two participants will engage in four distinct conversational tasks, including getting to know each other, free discussions, structured dialogues, and emotional interactions. In the second part, the participants will answer several questionnaires and perform neuropsychological tests in collaboration with an experimenter

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria
  • diagnosis of schizophrenia according to the DSM-V
  • being able to read, speak and understand french
  • giving eclaired consent
Exclusion Criteria
  • history of head trauma
  • history of neurological conditions (epilespsy, multiple sclerosis, parkinson's disease, amyotrophic lateral sclerosis, huntington's disease, stroke)
  • substance use
  • pregnant women

Healthy controls :

Inclusion Criteria:

  • being able to read, speak and understand french
  • giving eclaired consent

Exclusion Criteria:

  • diagnosis of psychosis
  • history of head trauma
  • history of neurological conditions (epilespsy, multiple sclerosis, parkinson's disease, amyotrophic lateral sclerosis, huntington's disease, stroke)
  • substance use
  • pregnant women

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
dyad schizophrenia and interacting partnerSocial interactionsocial interaction between an individual with a diagnosis of schizophrenia and his interacting partner
dyad healthy subject and interacting partnerSocial interactionsocial interaction between a healthy subject and his interacting partner
Primary Outcome Measures
NameTimeMethod
interpersonal synchronization4x6 minutes

synchronization between body movements of two interacting partners

intrapersonal synchronization4x6 minutes

synchronization between voice and body movements of one individual

Secondary Outcome Measures
NameTimeMethod
correlation between primary outcomes and individuals with schizophrenia medications4x6 minutes
correlation between synchronization and willingness to continue the interaction4x6 minutes

Trial Locations

Locations (1)

Montpellier University Hospital

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Montpellier, France

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