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Trial registered on ANZCTR
Registration number
ACTRN12617000939392
Ethics application status
Approved
Date submitted
20/06/2017
Date registered
28/06/2017
Date last updated
20/07/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Testing the performance of UV stickers for effective sunscreen use in Air and Water in healthy adults
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Scientific title
A Randomized Clinical Trial to Qualify “SPOT” UV stickers in Air and Water by healthy adults
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Secondary ID [1]
292238
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
sunburn
303737
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sun exposure
303738
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Condition category
Condition code
Skin
303111
303111
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0
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Other skin conditions
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention Groups:
There are two arms:
Arm 1: Arm 1 is the dry group, and will apply sunscreen once only at the beginning of the test session and UV SPOT indicating stickers on their lower legs, and be swabbed every 20 minutes for 7 cycles. The research assistant will apply the sunscreen on to the participant over the UV SPOT indicating stickers and lower leg to ensure adequate surface coverage.
Arm 2: Arm 2 will apply sunscreen once only at the beginning of the test session and UV SPOT indicating stickers on their lower legs, with the addition of having at least their lower legs in the pool for 20 minutes each cycle, with a rest break in between (i.e 20 minutes in the pool followed by 10 minutes rest out of the pool, repeated for 7 cycles). The research assistant will apply the sunscreen on to the participant over the UV SPOT indicating stickers and lower leg to ensure adequate surface coverage. Participants will be asked to wait 15 minutes for the sunscreen to soak in before entering the water. Participants can swim in the pool or sit on the edge of the pool with their lower legs submerged in the water.
Participants in both arms will receive 8 spots applied to their legs at the beginning of the test session. The data collection process (7 cycles) for both arms will take up to 4-5 hours to complete.
The sunscreen provided to both arms will be a high quality SPF 50+ water resistant 80min+ sunscreen that conforms to the Australian Standard. Participants will be required to use the sunscreen provided by the research team. Both groups will be indoors for the duration of the study at the Queensland University of Technology. Participants will not be testing the UV SPOT indicating stickers in direct sunlight. The UV SPOT indicating stickers will be removed from the participant by the research assistant, and placed in the sun for assessment between 11am-1pm when the UV index is above 3. All participants will be supervised by the research team during the intervention to ensure intervention adherence. Lifeguards are available at the indoor pool to ensure the swimmers safety at all times.
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Intervention code [1]
298399
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Prevention
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Comparator / control treatment
The sunscreen concentration on the skin is the reference field. The sunscreen concentration on the UV SPOT indicating stickers, will be compared to the participants sunscreen concentration on their skin.
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Control group
Active
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Outcomes
Primary outcome [1]
302488
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Correlate the amount of sunscreen on the participant’s skin to the amount of sunscreen on the UV SPOT indicating stickers .
The participants skin is swabbed using a 70%w/w 1sq" Rubbing Alcohol Swab, manufactured by BD. The technician wipes the swab over a 10cm^2 area five times, turns the swab around, and wipes 5 more times. The swab is analyzed outside of the testing environment using UV-Vis Spectroscopy to quantify the concentration of sunscreen on the skin. This swabbing procedure was based off of a similar procedure used by Bauer et al 2010 in the Journal Photochemistry and Photobiology.
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Assessment method [1]
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Timepoint [1]
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24hrs to 2 days post commencement of intervention the UV SPOT indicating stickers will be assessed in direct sunlight.
The amount of sunscreen on skin is measured at 8 time points (7 cycles total): 0, 20, 40, 60, 80, 100, 120, and 140 minutes after the sunscreen has been applied to the participant. At each of these time points, the skin will be swabbed using the Bauer procedure and the one SPOT sticker will be removed from the participant. At a later time point, all of the SPOT stickers will be brought into the sun by Dr. Hacker to have their colour analyzed using the NIX colour sensor and a photo taken of the SPOTs. Then, the SPOTs will be analyzed using UV-Vis Spectroscopy to quantify the amount of sunscreen on them.
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Secondary outcome [1]
336249
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Assess the colour UV SPOT indicating stickers changes when exposed to sunlight
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Assessment method [1]
336249
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Timepoint [1]
336249
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24hrs to 2 days post commencement of intervention the UV SPOT indicating stickers will be assessed in direct sunlight. The stickers have NIX Color Sensor data captured and a photo taken in direct sunlight.
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Eligibility
Key inclusion criteria
18+ Males and Females, healthy, able to communicate in English, able to participant in light physical activity.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Sunscreen allergies
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Randomisation by computer database (Redcap) will be used.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerised random-number generator
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
Our sample size was calculated in-line with the sunscreen standard testing sample size suggestion of 12 participants. We will have 12 participants for each (pool and dry) group giving a total of 24 participants. For a 95% CI (a=0.05) we would need 56 data points. Each participant ideally will return 8 data points, so this study design safely gathers enough data points to allow for meaningful conclusions to be drawn.
The skin swabs used in this study will allow for a quantitative analysis of the sunscreen correlation between the SPOT stickers and real human skin. Qualitative data will be gathered by a NIX color sensor in order to quantify the colour change using CIELAB colour values. A QUT statistician will independently analyse the data.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
30/06/2017
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Actual
30/06/2017
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Date of last participant enrolment
Anticipated
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Actual
18/07/2017
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Date of last data collection
Anticipated
30/09/2017
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Actual
19/07/2017
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Sample size
Target
24
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Accrual to date
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Final
24
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Recruitment in Australia
Recruitment state(s)
QLD
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Funding & Sponsors
Funding source category [1]
296784
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Commercial sector/Industry
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Name [1]
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Suncayr
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Address [1]
296784
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1/55 Shafston Ave, Kangaroo Point, QLD, 4059
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Country [1]
296784
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Australia
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Primary sponsor type
University
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Name
Queensland University of Technology
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Address
60 Musk Avenue, Kelvin Grove, QLD 4059
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Country
Australia
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Secondary sponsor category [1]
295768
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None
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Name [1]
295768
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Address [1]
295768
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Country [1]
295768
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
298008
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Queensland University of Technology
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Ethics committee address [1]
298008
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Institute of Health and Biomedical Innovation (IHBI), 60 Musk Ave, Kelvin Grove, QLD, 4059
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Ethics committee country [1]
298008
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Australia
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Date submitted for ethics approval [1]
298008
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Approval date [1]
298008
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16/06/2017
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Ethics approval number [1]
298008
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1700000387
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Summary
Brief summary
The proposed clinical trial aims to investigate the performance of the SPOT UV Indicating Stickers in pool water and on dry land. SPOT stickers are applied to a user’s skin before they apply their sunscreen, and their intended function is to change colour to warn users when their sunscreen is no longer protecting them. Participants in the study will be randomly assigned to one of the two activity groups (pool or dry) and will be wearing both sunscreen and SPOT stickers. Periodically, participants will have their SPOT stickers and skin swabbed, and the colour of the SPOT stickers measured. The aim of the study is to see that the amount of the sunscreen protecting the skin and the amount of sunscreen on the SPOT stickers are correlated. The study also will note that if a sufficient amount of sunscreen has worn off of a user’s skin that the SPOTs are changing colour to warn the user of overexposure to UV light. The study will be run over 3 weekend days, for 5 hours per participant session. The intended outcome is that SPOT stickers are seen to change colour should the amount of sunscreen protecting the users skin goes below a concentration of 0.5mg/cm3.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
75718
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Dr Elke Hacker
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Address
75718
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Queensland University of Technology, Institute of Health and Biomedical Innovation (IHBI), 60 Musk Ave, Kelvin Grove, QLD, 4059
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Country
75718
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Australia
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Phone
75718
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+61 7 3138 9674
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Fax
75718
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Email
75718
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[email protected]
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Contact person for public queries
Name
75719
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Elke Hacker
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Address
75719
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Queensland University of Technology, Institute of Health and Biomedical Innovation (IHBI), 60 Musk Ave, Kelvin Grove, QLD, 4059
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Country
75719
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Australia
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Phone
75719
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+61 7 3138 9674
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Fax
75719
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Email
75719
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[email protected]
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Contact person for scientific queries
Name
75720
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Elke Hacker
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Address
75720
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Queensland University of Technology, Institute of Health and Biomedical Innovation (IHBI), 60 Musk Ave, Kelvin Grove, QLD, 4059
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Country
75720
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Australia
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Phone
75720
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+61 7 3138 9674
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Fax
75720
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Email
75720
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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