NCT03432000

Brief Summary

People with schizophrenia show disturbances in the perception of time. Among these alterations are the perturbations of the temporal order judgment. They are characterized by the fact that, as opposed to the general population, people with schizophrenia require a longer time interval between two successive stimuli to estimate which of the two events appeared first. If these alterations are now well documented, their consequences remain little explored. Among these consequences could however appear distortions of the judgment of causality (likely to underlie certain delusional interpretations) as well as a distressing experience of loss of the continuity of the lived experience (that could contribute to the alterations basic of self-awareness).

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable schizophrenia

Timeline
Completed

Started Feb 2018

Typical duration for not_applicable schizophrenia

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2018

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

February 7, 2018

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 13, 2018

Completed
4.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 24, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 24, 2022

Completed
Last Updated

August 1, 2025

Status Verified

July 1, 2025

Enrollment Period

4.3 years

First QC Date

February 7, 2018

Last Update Submit

July 30, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Comparison of the scores obtained by subjects with schizophrenia vs. the controls for the causal tasks, according to the delays between stimuli (stopping the moving launcher and appearance of the static object).

    Michotte paradigm: evaluate the links (correlation) between perception of temporal sequencing and perception of causality using an adapted experimental paradigm

    eight months

Secondary Outcomes (1)

  • Comparisons of the scores obtained on the Time Experiment Rating Examination of Anomalous World Experience Scale (EAWE).

    eight months

Study Arms (2)

subjects with schizophrenia

EXPERIMENTAL

Performances on temporal task Subjective alterations of time perception in patients with an adapted scale (EAWE) Global symptomatology with PANSS (positive and negative symptom scale)

Other: Performances of patients and controls on temporal task

healthy subjects

SHAM COMPARATOR

Evaluate the links (correlation) between perception of temporal sequencing and perception of causality using an adapted experimental paradigm (Michotte paradigm) and to compare performance between healthy subjects and controls Investigate the existence of a correlation between these alterations and the peculiarities of the subjective experience of time (EAWE scale) in the group of subjects with schizophrenia

Other: Performances of patients and controls on temporal task

Interventions

To carry out this work, we will rely on an experimental paradigm (derived from Michotte's paradigm) which makes it possible to explore the links between temporal sequencing and perception of causality, validated in the normal subject. subjective consequences of these alterations will be explored using a phenomenological-inspired clinical scale (EAWE time-scale items)

healthy subjectssubjects with schizophrenia

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Subjects with schizophrenia:
  • Age from 18 to 45 years
  • Diagnosis of schizophrenia according to DSM V criteria
  • French mother tongue
  • Stable symptomatology
  • Normal or corrected visual acuity (\> 0.8 at Snellen scale) and normal color vision
  • Patients who gave informed consent to participate in the study
  • Control subjects (healthy volunteers):
  • Age from 18 to 45 years
  • Absence of neurological and psychiatric disorders
  • French mother tongue

You may not qualify if:

  • Recent addiction and abuse of cannabis or any other substance (according to DSM V criteria)
  • Neurological disorders of vascular, infectious or neurodegenerative origin
  • Taking somatic drugs with a cerebral or mental impact (eg corticosteroids)
  • Disabling sensory disturbances, and in particular visual acuity
  • Participation in a Neuro Cognitive Remediation Program
  • Schizophrenia resistant to neuroleptic treatments
  • Persons protected by law (pregnant women, minors, major under guardianship ...)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vial Veronique

Bron, Auvergne-Rhône-Alpes, 69678, France

Location

MeSH Terms

Conditions

Schizophrenia

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental Disorders

Study Officials

  • MARTIN BRICE

    CH LE VINATIER

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This study consists in: * evaluate the links (correlation) between perception of temporal sequencing and perception of causality using an adapted experimental paradigm (Michotte paradigm) and to compare performance between healthy subjects and controls * investigate the existence of a correlation between these alterations and the peculiarities of the subjective experience of time (EAWE scale) in the group of subjects with schizophrenia The measures that will be realized are: * Performances of patients and controls on temporal task * Subjective alterations of time perception in patients with an adapted scale (EAWE) * Global symptomatology with PANSS (positive and negative symptom scale)
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 7, 2018

First Posted

February 13, 2018

Study Start

February 1, 2018

Primary Completion

May 24, 2022

Study Completion

May 24, 2022

Last Updated

August 1, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations