- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04033731
Assessment of Stability of Behavioral and Neural Measures of Attention Networks Across Multiple Sessions
February 21, 2020 updated by: University of Florida
The purpose of this research study is to learn more about the stability over multiple recording sessions of brainwave activity during a computerized task that measures different types of attention.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Attention is the backbone of cognitive systems and is requisite for other cognitive processes vital to everyday functioning, such as memory, problem solving, language skills, and the cognitive control of behavior.
Impairments in attention can result from a variety of factors, such as brain injury, and neurodegenerative and neurodevelopmental disorders, as well as various psychopathologies.
A prominent multi-component model of visuospatial attention developed by Posner and colleagues conceptualizes visuospatial attention as an "organ system" comprised of three independent, yet interactive networks which include: 1) Alerting, the generation and maintenance of a vigilant state that facilitates the processing of an upcoming stimulus, 2) Orienting, the disengagement, shifting, and reallocation of attention to a spatial location, and 3) Executive control, the resolution of conflict among competing mutually-exclusive responses that enables selective focus.
To aid in understanding of attention, the Attention Network Test (ANT) was developed as a brief computerized measure of the efficiency of each of these networks and has been extensively used in a variety of healthy and clinical populations.
Several studies have examined differences in ERPs during the ANT in healthy aging and clinical populations such as ADHD, schizophrenia, and traumatic brain injury (TBI) but have not conducted repeated sessions of the task to evaluate changes over time.
While the ANT has been shown to be robustly sensitive to a range of cognitive and/or neuropsychological disorders, the reliability of the ANT across multiple sessions, particularly in terms of neural activity measures, has not been previously examined.
An important focus of the proposed research regards the stability of neural measures reflecting activity of each of three different attention networks.
One method for examining neural activity involves time locked electroencephalographic (EEG) recordings of brain activity or scalp-recorded brain event-related potentials (ERPs).
ERPs can provide insights into the neural correlates of cognitive processes elicited by an experimental task as well as the neural time course.
Particularly relevant to this study, the visual N1, a negative-going ERP deflection occurring ~150-200 milliseconds (ms) post-stimulus.
N1 amplitude is considered to index attentional allocation.
Additionally, a later-occurring positive-going deflection occurring ~300-ms post-stimulus, P3, reflects processes associated with stimulus evaluation and categorization.
Previous research in our lab has shown that N1 and P3 are differentially sensitive to attention network functioning probed using the ANT in neurologically-healthy controls and are sensitive to attentional impairment in TBI survivors.
Thus, the study team will focus on the stability of N1 and P3 waveforms across the 4 sessions.
Previous studies have examined reliability and stability of behavioral measures of the ANT by evaluating the reliability of reaction time (RT) and error rates over multiple sessions.
Ishigami reported good temporal stability of network scores across 10 sessions, although some practice effects were seen in orienting and executive-control attention networks.
Importantly, no prior work has examined the temporal stability of ERPs with repeated ANT performance, which is among the primary aims of the proposed research.
Finally, in an exploratory manner, the investigators will extend findings from one of our earlier studies demonstrating altitudinal attentional biases for upper vertical space in healthy participants and the absence of such biases in TBI survivors.
Specifically, the investigators will examine which of three attentional networks are sensitive to such biases in healthy controls and determine the ERP signatures of these biases.
Study Type
Observational
Enrollment (Actual)
16
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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Florida
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Gainesville, Florida, United States, 32611
- College of Public Health and Health Professions, University of Florida
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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
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Healthy Controls
Description
Inclusion Criteria:
- right-hand dominant
- Native English speakers
- with normal or corrected-to-normal vision
Exclusion Criteria:
- Not right-hand dominant
- Does not speak english as a native language
- No history of neurological disorder such as stroke, epilepsy or chronic seizure disorder, traumatic brain injury or concussion, psychiatric disorder such as schizophrenia, bipolar disorder, major depression or anxiety disorder, any psychiatric inpatient hospitalization for any of these disorders, or previously diagnosed learning disability
- Currently taking any prescribed medications for anxiety, depression, or seizures
- Alcohol use more than 3 days a week
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Controls
Participants will include 15 healthy men and women aged 18-40 years, right-hand dominant, Native English speakers, with normal or corrected-to-normal vision.
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The Attention Network Test (ANT) is a computerized cognitive task designed to efficiently probe three independent but interactive attentional networks (alerting, orienting, executive control) in a single task paradigm.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in the temporal stability of behavioral measures of three attention networks: change in reaction time across four sessions
Time Frame: Week 1; Week 2; Week 3; Week 4
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The Attention Network Task (ANT) combines a covert cuing paradigm with a classic flanker task to behaviorally probe independent but interactive components of attention.
These distinct components of attention are: alerting, orienting, and executive control.
These facets of attention will be assessed at 4 time points scheduled 1 week apart as follows: ANT Alerting Reaction Time score, ANT Orienting Reaction Time score and ANT Executive-control Reaction Time score.
The lower the score the faster the reaction time.
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Week 1; Week 2; Week 3; Week 4
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Change in the temporal stability of neural measures of three attention networks using scalp-recorded electroencephalography (EEG)
Time Frame: Week 1; Week 2; Week 3; Week 4
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Scalp-recorded brain event related potentials (ERP) will be acquired from 64 EEG sensors while participants perform the ANT reflecting alerting, orienting, and executive control components of attention.
These facets of attention will be assessed at 4 time points scheduled 1 week apart.
ANT alerting will be interrogated by examining the amplitude of the P300 component of the ERP in microvolts, as will orienting and executive-control.
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Week 1; Week 2; Week 3; Week 4
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: William Perlstein, PhD, University of Florida
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 (Actual)
January 31, 2019
Primary Completion (Actual)
November 8, 2019
Study Completion (Actual)
November 8, 2019
Study Registration Dates
First Submitted
July 19, 2019
First Submitted That Met QC Criteria
July 25, 2019
First Posted (Actual)
July 26, 2019
Study Record Updates
Last Update Posted (Actual)
February 24, 2020
Last Update Submitted That Met QC Criteria
February 21, 2020
Last Verified
February 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB201600188
- 0217BBRC-02 (Other Grant/Funding Number: *NF/SGVHS Malcom Randall VA Medical Cent)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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