Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
40 participants
OBSERVATIONAL
2024-01-01
2024-12-01
Brief Summary
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Detailed Description
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The aims of the study are to evaluate executive functions at the start and at the end of a working day and to understand theirs relationship with anxiety, perceived stress levels and physiological changes in sympathetic activity.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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eSense device
eSense device for monitoring electrodermal activity. Visual analogic scale (VAS) for pain and discomfort; TOL-R tests for investigating working performances.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Written informed consent obtained
Exclusion Criteria
* Neurological disorders
* Suffering from high blood pressure
18 Years
ALL
No
Sponsors
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University of Padova
OTHER
Responsible Party
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Annalisa Boscolo
Principal investigator
Locations
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Clinica Odontoiatrica
Padua, , Italy
Countries
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Other Identifiers
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Stress study
Identifier Type: -
Identifier Source: org_study_id