Skip to content

Comparison Of Video-based Versus Written Patient Education on Sunscreen

Comparison of Video-based Versus Written Patient Education on Sunscreen Behavior

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00826306
Enrollment
94
Registered
2009-01-22
Start date
2009-01-31
Completion date
2009-08-31
Last updated
2015-04-16

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

Conditions

Dermatology Disease, Skin Cancer

Keywords

patient education, dermatology patient education, sunscreen, sunscreen education, skin cancer

Brief summary

The purpose of this study is to compare the effect of video-based patient education with written instruction on subjects' adherence to sunscreen application.

Detailed description

We plan to conduct a randomized, controlled trial comparing the effect of video-based patient education with written instruction on subjects' adherence to sunscreen application. Subjects randomized to the video-based education arm will be instructed to watch a video on the importance of sunscreen application and the proper technique of applying sunscreen. Subjects randomized to the written education arm will receive written information on the importance of sunscreen application and the proper technique of applying sunscreen. The contents of the video and the written educational materials will be comparable. At the end of the study period, 3 months later, subjects will be interviewed via telephone regarding their sunscreen application behavior during the last month of the study period. Subjects will also be interviewed regarding their comprehension and attitude towards video-based and written education materials.

Interventions

In the experimental arm, the intervention is the video-based patient educational material on sunscreen. In the active comparison arm (control arm), the comparison intervention is written patient educational material on sunscreen.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years of age or older at time of consent, may be men or women. * Able to adhere to the study visit schedule and other protocol requirements. * Capable of giving informed consent.

Exclusion criteria

* Non-English speaking individuals * Individuals with a known allergy to sunscreens * Individuals with a history of psoriasis, because phototherapy has been shown to be beneficial for their skin condition

Design outcomes

Primary

MeasureTime frame
Sunscreen application behavior.3 months

Secondary

MeasureTime frame
Subjects' comprehension and attitude towards video-based and written education materials.3 months

Countries

United States

Outcome results

None listed

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