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Randomized Pilot Study Evaluating Isopropyl Alcohol and UVC Rays in Disinfection of Cell Phones

Randomized Experimental Pilot Study Evaluating Isopropyl Alcohol and UVC Rays in Disinfection of Cell Phones of Healthcare Workers.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06194903
Acronym
SaniPhone
Enrollment
72
Registered
2024-01-08
Start date
2024-02-01
Completion date
2024-04-01
Last updated
2024-09-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cross Infection

Keywords

cross infection, high touch surfaces, cellphone, disinfection, isopropyl alcohol, UVC

Brief summary

Cell phones have become a fundamental accessory of our lives and clinical practice, often kept in contact with the body. Since most modern smartphones are equipped with touch screens, they can serve the function of reservoirs for pathogenic microorganisms; moreover, they can be the means of transmission of such microorganisms from the environment to humans. 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.

Interventions

DEVICEisopropyl 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.

DEVICEUVC 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.

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Be a healthcare provider in the departments of Neonatology, Geriatric Internal Medicine, Nephrology, Anesthesia, Resuscitation, Intensive Care Unit at Fondazione Policlinico Universitario A.Gemelli IRCCS * 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 a healthcare worker in the departments of Neonatology, Geriatric Internal Medicine, Nephrology, Anesthesia, Resuscitation, Intensive Care Unit at Fondazione Policlinico Universitario A.Gemelli IRCCS * 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

Design outcomes

Primary

MeasureTime frameDescription
Average total bacterial load at 3 hours after sanitizationSamples will be collected immediately before and immediately after sanitisation and 3 hours after sanitisation.The primary objective of the pilot study is to obtain preliminary data on the average total bacterial load at 3 hours after the sanitization intervention (70% isopropyl alcohol wipes or UVC box). These data will allow appropriate sizing of a subsequent trial to evaluate whether, on the cell phones of health care workers at the Fondazione Policlinico Universitario A. Gemelli IRCCS, wipes impregnated with 70% isopropyl alcohol are more effective than UVC ray boxes in reducing total bacterial load at 3 hours after sanitization for both isopropyl alcohol wipes and UVC box

Secondary

MeasureTime frameDescription
Change in the average total bacterial load at 3 hours after sanitizationSamples will be collected immediately before and immediately after sanitisation and 3 hours after sanitisationExplore the change in the average total bacterial load at 3 hours after sanitization interventions compared with the value recorded before sanitisation for both isopropyl alcohol wipes and UVC box.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026