- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07650890
Neurocognitive Performance in Public Officials
A Comparison of Neurocognitive Performance in Armed and Unarmed Public Officials
Public employees are exposed to varying levels of cognitive, physical, and psychosocial demands depending on the nature of their duties. In particular, armed public employees work under conditions that require rapid responses to environmental stimuli, effective use of attentional processes, and accurate decision-making within a limited time. These occupational demands may influence reaction time, neurocognitive performance, quality of life, and activity-role balance. Therefore, the aim of this study was to compare the neurocognitive performance of armed and unarmed public employees.
A total of 82 public employees, including 41 armed and 41 unarmed participants, were included in the study. Reaction time performance was assessed using the Light Trainer system. Neurocognitive performance was evaluated using the Stroop Test and the Digit Span Test. Quality of life was assessed using the Short Form-36 Health Survey (SF-36), and activity-role balance was evaluated using the Activity Role Balance Questionnaire.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Istanbul, Turkey (Türkiye)
- AtLAs Universty
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged between 25 and 35 years.
- Actively employed as a public official for at least 3 years.
- A score of 26 or higher on the Mini-Mental State Examination (MMSE).
- Currently employed full-time.
- Able to understand and speak Turkish.
- Willing to participate in the study and provide informed consent.
Exclusion Criteria:
- Presence of a diagnosed neurological or psychiatric disorder.
- History of traumatic brain injury or severe head trauma within the past 6 months.
- Presence of an orthopedic condition or injury that may affect upper or lower extremity function.
- Presence of visual, auditory, or other sensory impairments that may interfere with test performance.
- Current use of medications or history of substance use that may affect cognitive performance.
- Previous exposure to or administration of the neurocognitive tests used in this study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Armed Public Officials
Public officials who are legally authorized to carry firearms as part of their occupational duties.
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Unarmed Public Officials
Public officials who are not authorized to carry firearms as part of their occupational duties.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Muscle Reaction Time
Time Frame: Baseline (single assessment)
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Light Trainer® system, which consists of a wireless lighting system with LED pods and a central controller.
The participants were seated with their hands on the table, 40 cm apart, palms down, and elbows at 90°.
The Light Trainer was positioned centrally 20 cm away from each hand.
When the pod was illuminated, the participants were instructed to turn off the light as quickly as possible by touching it.
Light activation was randomized to avoid predictability, requiring participants to respond based on light cues each time.
In the first task, the participants used their dominant hand to turn off the light as quickly as possible.
In the second task, they responded to a light signal by deactivating a predetermined light from two different colors using their dominant hand.
Scale Range: No minimum or maximum value in milliseconds (lower time is better).
Interpretation: Lower reaction times signify better outcomes, as they reflect faster muscle response to visual stimuli.
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Baseline (single assessment)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Digit Span Test Performance
Time Frame: Baseline (single assessment)
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Assesses attention and working memory using the Digit Span Test.
Performance is determined by the maximum number of digits correctly recalled in forward and backward sequences, with higher scores indicating better cognitive performance.
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Baseline (single assessment)
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Stroop Test Performance
Time Frame: Baseline (single assessment)
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Assesses selective attention, cognitive flexibility, inhibitory control, and processing speed using the Stroop Test.
Performance is determined by the time required to complete the task and the number of errors made during the assessment.
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Baseline (single assessment)
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Quality of Life (SF-36)
Time Frame: Baseline (single assessment)
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Assesses health-related quality of life using the Short Form-36 Health Survey (SF-36).
The SF-36 consists of 36 items and generates scores ranging from 0 to 100 for each domain, with higher scores indicating better health-related quality of life and better perceived health status across physical and mental health domains.
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Baseline (single assessment)
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Activity-Role Balance Questionnaire
Time Frame: Baseline (single assessment)
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Assesses the perceived balance between daily activities and life roles using the Activity-Role Balance Questionnaire (ARBQ).
Scores range from 1 to 5, with higher scores indicating a more satisfactory balance between occupational roles and daily activities.
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Baseline (single assessment)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- ID_M_003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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