Randomized Pilot Study Evaluating Isopropyl Alcohol and UVC Rays in Disinfection of Cell Phones
NCT ID: NCT06194903
Last Updated: 2024-09-27
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
NA
72 participants
INTERVENTIONAL
2024-02-01
2024-04-01
Brief Summary
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A number of observational studies are available in the literature evaluating the effectiveness of various sanitization methods in reducing the bacterial load of high-touch devices, both chemical and physical.
To our knowledge, no real-world evidence is available comparing the residual effect of the two methods on the bacterial load of cell phones, since all available studies are carried out in the laboratory, with inoculums of predetermined bacterial loads whose suppression by the disinfectant is monitored over time, and involve laptops, tablets and keyboards.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Cellphones treated with isopropyl alcohol wipes
isopropyl alcohol wipes
cellphones will be sanitised with isopropyl alcohol wipes and total bacterial load will be assessed immediately before sanitation, immediately after sanitation and 3 hours after sanitation.
Cellphones treated with UVC box
UVC box
cellphones will be sanitised in a UVC box and total bacterial load will be assessed immediately before sanitation, immediately after sanitation and 3 hours after sanitation.
Interventions
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isopropyl alcohol wipes
cellphones will be sanitised with isopropyl alcohol wipes and total bacterial load will be assessed immediately before sanitation, immediately after sanitation and 3 hours after sanitation.
UVC box
cellphones will be sanitised in a UVC box and total bacterial load will be assessed immediately before sanitation, immediately after sanitation and 3 hours after sanitation.
Eligibility Criteria
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Inclusion Criteria
* Own a smartphone
* Carry one's smartphone for the duration of the work shift (8 hours)
* Give consent to participate in the study
* Be willing to report 3 hours after sanitisation for follow-up sampling
Exclusion Criteria
* Not to be on work shift during surveys
* Not to carry one's smartphone for the duration of the work shift (8 hours)
* Not to give consent to participate in the study
* Not to be willing to report 3 hours after sanitisation for follow-up sampling
ALL
Yes
Sponsors
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Fondazione Policlinico Universitario Agostino Gemelli IRCCS
OTHER
Responsible Party
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Laurenti Patrizia
Professor
Locations
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Fondazione Policlinico Universitario "A. Gemelli" IRCCS
Rome, , Italy
Countries
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Other Identifiers
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6015
Identifier Type: -
Identifier Source: org_study_id
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