Schizophrenia Clinical Trial
Official title:
Perception Processing in Schizophrenia Patients and Normal Population.
NCT number | NCT01298349 |
Other study ID # | 104-10 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | February 2011 |
Est. completion date | December 2017 |
Verified date | February 2020 |
Source | HaEmek Medical Center, Israel |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 71 |
Est. completion date | December 2017 |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - 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 Exclusion Criteria: - deterioration of the disorder - subject will |
Country | Name | City | State |
---|---|---|---|
Israel | Haemek Medical Center | Afula |
Lead Sponsor | Collaborator |
---|---|
HaEmek Medical Center, Israel |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | |
Primary | 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. | |
Primary | Performance in Experiment 2: Error Rate (%) | Percentage of Errors; The ratio between number of errors and the total number of responses. | 2 weeks. |
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