- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01330537
Exploring the Visual Sensitivity for Topological Properties in Newborn Infants
January 27, 2021 updated by: Sarina Hui-Lin Chien, China Medical University Hospital
The topological perception theory proposed a precise description for how one organizes the visual world that eliminates the vagueness of subjective phenomenology.
In addition, the topological theory challenges the dominant computational view on the part-to-whole hierarchy of visual information processing.
Lines of evidence from adult psychophysics, brain imaging data, and even honeybee's behavior have supported the notion that the global topological properties are the very primitives of visual representation.
However, the question of how the sensitivity to topological properties originates during development has not been explored much.
In a previous study, the investigators found that 2- to 6 month old infants could reliably discriminate stimuli based on topological differences, but failed to do so based on geometric differences.
Using familiarization/novelty preference procedure, the present study intends to explore the visual sensitivity for topological properties in newborn infants.
Experiment 1 focuses on whether neonates can discriminate a disk (no hole) and a ring (with a hole) that are topologically different, and/or a disk (no hole) and a triangle (no hole) that are geometrically different.
Experiment 2 focuses on whether neonates can detect a change in the number of holes and/or the size of the hole.
If newborn infants are only sensitive to topological properties and not to geometric properties, this will be a strong proof for the claim that topological property is the very "primitive" visual representation at empirical as well as theoretical level.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Taichung, Taiwan, 40402
- China Medical University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 hours to 2 weeks (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
full-term and healthy newborns
Description
Inclusion Criteria:
- full-term and healthy newborns
Exclusion Criteria:
- Eye illnesses or other physical problems
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Sarina Hui-Lin Chien, PhD, Graduate Institute of Neural and Cognitive Sciences, China Medical University, Taiwan
- Principal Investigator: Bai-Horng Su, M.D., China Medical University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2011
Primary Completion (Actual)
February 1, 2013
Study Completion (Actual)
March 1, 2013
Study Registration Dates
First Submitted
April 5, 2011
First Submitted That Met QC Criteria
April 6, 2011
First Posted (Estimate)
April 7, 2011
Study Record Updates
Last Update Posted (Actual)
January 28, 2021
Last Update Submitted That Met QC Criteria
January 27, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DMR100-IRB-019
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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