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CompletedNCT02874482SAILLANCE1Updated Aug 26, 2020

Cognitive and Emotional Factors in Visual Exploration Among Patients With Schizophrenia

An observational study in Schizophrenia, sponsored by University Hospital, Lille. Completed at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-08-26.

Sponsored by University Hospital, Lille · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
42
Ages
18 Years and older
Sex
All
01

Study summary

Background:

Patients with schizophrenia are abnormally disturbed by information onsets, which may result in a disadvantage in filtering relevant information. It seems that they accord the same importance to all objects in a scene without taking into account the relevance of objects (cognitive salience) or their emotional charge (salience emotional).

The paradigm of change blindness offers the interesting possibility of studying sensitivity to the sudden irruption of visual information with ecological stimuli in schizophrenia. An increased attentional capture by the irruption of visual information would suggest better performance in patients than in healthy controls. Moreover, patients are disturbed to processing of emotional information, in this way we would like to measure the impact of emotional salience on the visual exploration.

Main aim:

The main objective is to evaluate, if patients with schizophrenia quickly detect changes occurring on irrelevant objects in the understanding of the scene.

Secondary objectives:

To evaluate in patients with schizophrenia the impact of emotional salience using the same paradigm.

To separate an explicit response (motors responses) with an implicit response (eye tracking measures).

Methodology:

30 patients with schizophrenia and 30 healthy controls were asked to detect changes in 96 scenes with 0 or 1 change (neutral or emotional changes). We will measure the participants' speed and accuracy in explicitly reporting the changes via motor responses and their capacity to implicitly detect changes via eye movements.

Read the detailed description

This study will include one visit:

  • Written consent will be obtained from all participants
  • Inclusion and exclusion criteria will be checked
  • An ophthalmologic test, a pregnancy test, a alcohol test and a salivary test will be realized
  • Various symptoms will be assessed with the PANSS (Positive And Negative Syndrome Scale for schizophrenia) and the UPDRS (Unified Parkinson Disease Rating Scale for patients, the MOCA (Montreal Cognitive Assessment), The HAD (Hospital Anxiety and Depression Scale) and the MINI (Mini International Neuropsychiatric Interview) for all participants.
  • The task will be divided in two parts:

A visuo-spatial task allowing to record saccadic eye movements (approximately 10 min).

The change blindness session lasted approximately 20 min.

02

Conditions studied

  • Schizophrenia

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Keywords

  • Schizophrenia
  • Change blindness
  • Eye tracking
  • Implicit response
03

In context

Schizophrenia

3,471 studies on the registry are indexed under Schizophrenia; 472 are open to participants now.

This study's enrollment of 42 is below the median of 178 across 491 observational studies indexed under Schizophrenia.

Browse Schizophrenia studies →

Lead sponsor

University Hospital, Lille is the lead sponsor of 625 studies on the registry; 141 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

30 patients with schizophrenia and 30 healthy controls

Inclusion criteria

  • Normal or corrected vision
  • Affiliate to a social security system
  • For group of patients with schizophrenia : diagnosis of schizophrenia based on the standard DSM-IV criteria and patients will be clinically stable at the testing time

Exclusion criteria

Exclusion Criteria:

  • History of neurological illness
  • Pregnant and nursing women
  • Drugs use in the last 24 hours
  • Acute ocular disorder
  • Under tutorship, curatorship or deprived of liberty
  • For controls group : be free DSM-IV axis-I diagnoses according the MINI test.
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
42 participants (actual)
Patient registry
No

Groups and cohorts

  • Patients with schizophrenia

    30 patients with schizophrenia (diagnosis based on the standard DSM criteria)

  • Controls

    30 healthy controls without any psychiatric or neurological diagnosis

06

What researchers measure

Primary outcomes

  1. response time

    The explicit response of the participants will be measure behaviourally by response time before the detection of neutral stimuli.

    Time frame: 42 months

Secondary outcomes

  1. sensitivity index

    Performances will be measure by a sensitivity index (D prime) which considers the number of correct detections compared with the missed detections and false alarms; thus it evaluates the capacity to discriminate the signal against a background noise.

    Time frame: 42 months

  2. implicit response

    The implicit response will be measure by the localization and duration of fixations

    Time frame: 42 months

  3. emotional response

    The emotional response will be measure by the localization, duration of fixations and performances for the detection of emotional stimuli

    Time frame: 42 months

07

Study locations

1 site
  • University Hospital, Lille
    Lille, 59037, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 26, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02874482
Lead sponsor
University Hospital, Lille
Responsible party
Sponsor
First posted
Aug 22, 2016
Start date
Jul 2014
Primary completion
Nov 17, 2019
Completion
Nov 17, 2019
Last update
Aug 26, 2020

Study contacts

Guillaume VAIVA
principal investigator · University Hospital, Lille

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.

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