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Implementing and evaluating Ultraviolet-C mobile phone sanitisation for infection control in the intensive care unit.

The acceptability, sustainability, and perceived utility of Ultraviolet-C phone sanitisation as a supplementary infection control measure used by healthcare workers in the intensive care unit.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626001152314
Enrollment
50
Registered
2026-09-16
Start date
2027-02-01
Completion date
2027-05-01
Last updated
2026-09-16

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

Conditions

None listed

Brief summary

Mobile phones are ubiquitous in healthcare settings as patients, visitors and healthcare workers use them frequently. Mobile phones can carry harmful microbes in healthcare settings, especially in the intensive care unit, and may potentially be putting patients at risk of contracting healthcare-associated infections. Therefore, mobile phone sanitisation solutions are required for healthcare settings, and ultraviolet-C (UV-C) devices offer a promising solution to this problem. However, it is yet to be investigated whether healthcare workers will be willing to use UV-C devices frequently to disinfect their phones at work. Hence, this study aims to implement a UV-C device in a real-world intensive care unit, and evaluate whether it is accepted and utilised by healthcare workers.

Interventions

A Glissner Cleanphone Ultraviolet-C (UV-C) device will be implemented in a prominent location in the intensive care unit for healthcare workers to self-administer cleaning of their mobile phones. This device applies UV-C radiation to the full 360-degree surface of mobile phones and is a touchless device, meaning no cross-contamination with clean hands. The device is 30cm tall, 26cm wide, and 14cm deep, making it portable and feasible to implement in clinical environments. Furthermore, this devic

A Glissner Cleanphone Ultraviolet-C (UV-C) device will be implemented in a prominent location in the intensive care unit for healthcare workers to self-administer cleaning of their mobile phones. This device applies UV-C radiation to the full 360-degree surface of mobile phones and is a touchless device, meaning no cross-contamination with clean hands. The device is 30cm tall, 26cm wide, and 14cm deep, making it portable and feasible to implement in clinical environments. Furthermore, this device uses an ultra-rapid cleaning time of only 10-seconds per application. Participants can use the device as often as they like throughout the implementation period and will be encouraged to do so via informational posters placed in the intensive care unit, and communication via meetings, emails, and in-services. Each Glissner Cleanphone device has been retrofitted with a magnetic counter which will record the number of times the device is utilised. This data will be downloaded from the device by the research team after the first 48 hours of implementation, and then weekly to track the amount of device usage over time, and map trends of acceptability, sustainability, and perceived utility. It is anticipated that the overall duration of implementation will be approximately 3-months This study will employ an iterative quality improvement methodology with the Plan-Do-Study-Act (PDSA) method used as the overarching implementation process. The barriers and facilitators of behaviour change and implementation which were identified through a previous staff survey will inform the preliminary iterative cycles of the PDSA method. Acceptability, sustainability, and perceived utility will be measured following the first PDSA cycle by a follow-up staff survey.

Sponsors

The Prince Charles Hospital
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adult (greater than or equal to 18 years of age) healthcare workers within the intensive care unit at The Prince Charles Hospital and St Andrew’s War Memorial Hospital.

Exclusion criteria

Individuals who do not wish to be part of the study / do not provide consent.

Outcome results

None listed

Source: ANZCTR · Data processed: Sep 16, 2026