UV Sensor in Patients With Actinic Keratosis

NCT ID: NCT05481073

Last Updated: 2022-11-14

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-06-13

Study Completion Date

2022-09-01

Brief Summary

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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

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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.

Conditions

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Keratosis, Actinic

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

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UV sensor

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

Intervention Type DEVICE

Eligibility Criteria

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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.
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Almirall, S.A.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Dermatology Unit (Hospital Clinic)

Barcelona, , Spain

Site Status

Countries

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Spain

Other Identifiers

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Usability UV sensor study

Identifier Type: -

Identifier Source: org_study_id

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