NCT01298349

Brief Summary

The present study aimed to examine face and object perception processes in schizophrenic patients. Schizophrenia is associated with deficits in visual processing that represent a key feature in the disorder. Previous studies have shown that schizophrenics exhibit deficits in a variety of facial-processing tasks (e.g., face recognition, recognition of facial expressions), that may severely hinder the patients' interpersonal and social skills. Some investigators have attributed these deficits to impairments in configural processing in schizophrenia. That is, an impairment in the ability to process the spatial relations between the constituent parts of a configuration (e.g., the spacing between the eyes of a given face). To date, studies aimed to investigate this possibility (e.g., Schwartz et al., 2002; Yong-Wook et al., 2008) yielded conflicting results. Additionally, it is not yet clear whether the hypothesized impairment in configural processing is restricted to faces, or whether it is more general in nature and applies to objects as well.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
71

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2011

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

December 2, 2010

Completed
2 months until next milestone

Study Start

First participant enrolled

February 1, 2011

Completed
16 days until next milestone

First Posted

Study publicly available on registry

February 17, 2011

Completed
5.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2016

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2017

Completed
Last Updated

February 17, 2020

Status Verified

February 1, 2020

Enrollment Period

5.8 years

First QC Date

December 2, 2010

Last Update Submit

February 12, 2020

Conditions

Outcome Measures

Primary Outcomes (3)

  • Performance in Experiment 1: Probability of Global Perception (%)

    The probabilities (in percentage) of choosing the comparison figure having the same configuration as the standard figure. That is, the ratio between the number of trials in which participants chose the comparison figure as having the same configuration as the standard figure, and the total number of trials.

    2 weeks.

  • Performance in Experiment 2: Response Time (milliseconds)

    Response Time in milliseconds; will be measured from stimulus onset on screen until prticipant's response.

    2 weeks.

  • Performance in Experiment 2: Error Rate (%)

    Percentage of Errors; The ratio between number of errors and the total number of responses.

    2 weeks.

Study Arms (2)

schizophrenic patients

normal population

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

patients diagnosed with schizophrenia or schizo-affective disorder according to DSM4 and normal population with no psychiatric history

You may qualify if:

  • schizophrenia or schizo-affective disorder
  • normal population with no psychiatric history
  • Stable medication for at least a month before participating in the study
  • subjects must have normal vision or revised

You may not qualify if:

  • deterioration of the disorder
  • subject will

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Haemek Medical Center

Afula, Israel

Location

MeSH Terms

Conditions

Schizophrenia

Condition Hierarchy (Ancestors)

Schizophrenia Spectrum and Other Psychotic DisordersMental Disorders

Study Officials

  • Boaz Bloch, MD

    Haemek Mediacl Center

    PRINCIPAL INVESTIGATOR
  • Alon Reshef, MD

    haemek medical center

    STUDY CHAIR
  • Rama Amishav, Phd

    haemek medical center

    STUDY CHAIR

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 2, 2010

First Posted

February 17, 2011

Study Start

February 1, 2011

Primary Completion

December 1, 2016

Study Completion

December 1, 2017

Last Updated

February 17, 2020

Record last verified: 2020-02

Locations