Helping All Children be Safe Outdoors With Sun Protection
NCT ID: NCT02376517
Last Updated: 2015-09-17
Study Results
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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COMPLETED
NA
300 participants
INTERVENTIONAL
2015-05-31
2015-09-30
Brief Summary
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Detailed Description
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This is a 12-week summer pilot study. The research seeks to develop a multicomponent sun protection program that is feasible for family practice and pediatric clinicians to introduce with anticipatory guidance during well-child visits. The program will further be implemented through a sun protection read-along book in English and Spanish and weekly text message reminders.
The sun protection program will enable behavioral change by caregivers and children of all ethnic and racial backgrounds. Testing the feasibility of delivering the intervention in a family medicine or pediatric practice will allow assessment of accrual and retention rates in a racially/ethnically diverse population, and lead the way to dissemination of good practice.
Participant in this study will be asked to complete two in-person visits at an Advocate Medical Group pediatric clinic. These visits will take place over a four to six week period. The first visit, or Baseline, may be on the same day as the child's well-visit. The second visit, or Follow-Up, will take place at the same location as the Baseline.
Participants randomized to the intervention group will receive the educational program at Baseline, whereas participants in the control group will receive the educational program during Follow-Up.
At the first visit (Baseline), the participant will:
1. Complete an anonymous short self-administered questionnaire about knowledge of sun protection and the child's sun protection habits
2. Some participants will be asked to complete a survey about cultural affiliation.
3. Receive the educational program at the first visit if randomized to the intervention group.
At the second visit (Follow-Up), the participant will:
1. Complete an anonymous short self-administered questionnaire about knowledge of sun protection and the child's sun protection habits.
2. Receive the educational program at the second visit if randomized to the control group.
At the end of each visit, the amount of melanin (pigment) in the child's skin will be measured. This involves the use of a Mexameter, a device that lightly presses on the child's arm to take a reading (picture) of how much pigment there is in his/her skin. This is neither painful nor invasive.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SCREENING
NONE
Study Groups
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Educational program
Participants randomized to the intervention group will receive the educational program at the baseline visit.
Educational program
The educational program consists of a short (13 pages) read-along book in English and Spanish. This book presents sun protective practices at an appropriate level for 2-6 year old children to read with their parent or caregiver. A sun protective swim shirt, which provides a sun-protection factor (SPF) of over 50, for the child will be provided. Additionally, the parent will receive weekly text message reminders to practice sun protection.
Control
Participants randomized to the control group will receive the educational program at the follow-up visit.
No interventions assigned to this group
Interventions
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Educational program
The educational program consists of a short (13 pages) read-along book in English and Spanish. This book presents sun protective practices at an appropriate level for 2-6 year old children to read with their parent or caregiver. A sun protective swim shirt, which provides a sun-protection factor (SPF) of over 50, for the child will be provided. Additionally, the parent will receive weekly text message reminders to practice sun protection.
Eligibility Criteria
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Inclusion Criteria
* Is the parent of a 2-6 year old child attending a well-child visit
* If the parent present is female, she may be pregnant
* Are able to read in English and/or Spanish at a 6th grade level or higher
* Are able to receive text messages
Exclusion Criteria
* Unable to read in English and/or Spanish at a 6th grade level or higher
* Unable to receive text messages
* Unable to complete study procedures with eligible child
* Unable to return to clinic for a follow-up visit
18 Years
ALL
Yes
Sponsors
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Northwestern University
OTHER
Responsible Party
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June Robinson
Professor of Dermatology
Principal Investigators
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June K Robinson, MD
Role: PRINCIPAL_INVESTIGATOR
Northwestern University
Locations
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Northwestern University Feinberg School of Medicine Department of Dermatology
Chicago, Illinois, United States
Advocate Medical Group - Pediatric Clinics
Park Ridge, Illinois, United States
Countries
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References
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Ho BK, Reidy K, Huerta I, Dilley K, Crawford S, Hultgren BA, Mallett KA, Turrisi R, Robinson JK. Effectiveness of a Multicomponent Sun Protection Program for Young Children: A Randomized Clinical Trial. JAMA Pediatr. 2016 Apr;170(4):334-42. doi: 10.1001/jamapediatrics.2015.4373.
Other Identifiers
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STU00200215
Identifier Type: -
Identifier Source: org_study_id
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