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HealthyNCT05709743

Task Switching Between Target Templates During Visual Search in Healthy Adults

A study testing Experimental: Within-Subjects Attentional Information in people with Healthy, run by Lehigh University at 1 site in United States.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

In this line of research, the researchers having participants engage in task switching between tasks which require a positive (target) template, negative (distractor) template, or neutral (non-informative) template to the cognitive control factors associated with each template type during visual search. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
Experimental: Within-Subjects Attentional Information
Could I receive a placebo?
No, everyone receives an active treatment
How many people
24 participants
Where
1 siteUnited States
Study dates
12 Apr 2023to 17 Jun 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • normal or corrected to normal visual acuity, normal color vision

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site
  • Lehigh University

    Bethlehem, Pennsylvania, 18015

Other trials in United States

About this study

Official title: Task Switching Between Positive and Negative Target Templates During Visual Search in Healthy Adults

In this line of research, the researchers having participants engage in task switching between tasks which require a positive (target) template, negative (distractor) template, or neutral (non-informative) template to the cognitive control factors associated with each template type during visual search. This is a basic science study.

Read the detailed description

The researchers will have participants engage in task switching between tasks which require a positive (target) template, negative (distractor) template, or neutral (non-informative) template to the cognitive control factors associated with each template type during visual search. Looking for impacts of task switching helps to identify the components of the cognitive control system that overlap between different types of attentional templates. This is a basic science study.

Conditions
Healthy
Being tested
Experimental: Within-Subjects Attentional Information
Keywords
attention, visual search

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Experimental: Within-Subjects Attentional InformationBehavioural

    Also called Within-Subjects, all participants receive all interventions

    Behavioral: Visual Search Information Type (target or distractor information) Participants will have information about targets, distractors, or neither in different trials of the intervention.

Study groups in NCT05709743
Study groupRoleWhat they receive
Within-Subjects Attentional InformationExperimentalWithin-Subjects, all participants receive all interventions
Receives: Behavioral: Experimental: Within-Subjects Attentional Information

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Button Press Reaction Time

    Speed to respond correctly to the target- after participant finds the target shape on a computer screen, they press a button to indicate what shape they see

    Measured: One day (during testing)

  2. Button Press Accuracy

    Accuracy of responses to target item (% correct)- the researchers will measure whether the participants presses the correct button which corresponds to the target shape presented on the computer screen or the incorrect button

    Measured: One day (during testing)

  3. Eye Movements to Objects on Computer Screen

    Proportion (% of total) of eye movements directed to potential targets or distractors, measured with an Eye Link II eye tracker

    Measured: One day (during testing)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Feb 2023
  2. Study start12 Apr 2023
  3. Primary completion17 Feb 2025 (estimated)
  4. Study completion17 Jun 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Model description
All participants receive each level of visual information (target or distractor)
Masking
None (open label)
Enrolment
24 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05709743
Sponsor's protocol ID
4R15EY030247-01A1
Status last verified
Oct 2024
First submitted
24 Jan 2023
Last updated
9 Oct 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The researchers plan to share anonymized subject data on Open Science Framework.

Questions about this trial

What is this clinical trial studying?

A study testing Experimental: Within-Subjects Attentional Information in people with Healthy, run by Lehigh University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 9 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Button Press Reaction Time (time frame: One day (during testing)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Oct 2024.

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Clinical Trial NCT05709743 | AzTrials