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UV Sensor in Patients With Actinic Keratosis

Pilot Feasibility Study of Using UV Sensor in Patients With Actinic Keratosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05481073
Enrollment
10
Registered
2022-08-01
Start date
2022-06-13
Completion date
2022-09-01
Last updated
2022-11-14

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

Conditions

Keratosis, Actinic

Brief summary

To validate the use of Ultraviolet (UV) radiation sensor in patients with actinic keratosis, to identify barriers to its use in prospective longitudinal studies.

Detailed description

To prevent both acute and chronic damage from exposure to UV A and UV B radiation. Personal UV exposure can be assessed by portable sensors. Having an accurate awareness of one's own behavior (assessed by the accuracy of the UV sensor), can motivate and engage with skin protection.

Interventions

DEVICEUV sensor

Use of UV sensor to be informed about the sun exposure daily through a mobile application

Sponsors

Almirall, S.A.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\>=65 years presenting actinic keratosis on scalp and/or face

Exclusion criteria

Patients who, due to health problems or lifestyle habits, do not expose themselves regularly to UV radiation (outdoor) for at least one hour a day.

Design outcomes

Primary

MeasureTime frameDescription
QOL UV sensorUp to week 4Questionnaire will be carried out to qualitatively evaluate different aspects of the usability of the UV device, Minimum Value 0; Maximun Value 20, where higher value is the better.

Countries

Spain

Outcome results

None listed

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