Clinical Trials Directory

Trials / Completed

CompletedNCT01176955

A Novel Method to Improve Acne Outcomes

A Novel Method for Improving Acne Outcomes

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Wake Forest University · Academic / Other
Sex
All
Age
13 Years – 18 Years
Healthy volunteers
Not accepted

Summary

This is an investigator-blinded, prospective study of 20 subjects aged 13 through 18 with mild to moderate acne. Study subjects will be randomized to an internet survey group, in which an email link for a survey ascertaining the status of the subject's acne is sent weekly, or to a control group. All study subjects will use benzoyl peroxide 5% gel, and adherence and clinical improvement will be monitored over 12 weeks. The investigators hypothesis is that subjects in the internet survey group will have improved adherence to the study medication and clinical outcomes, because the weekly survey will remind subjects to use their medication.

Conditions

Interventions

TypeNameDescription
BEHAVIORALInternet surveyA weekly email link will be generated to an internet survey which questions subjects about their acne severity, compliance with the study medication, and attitudes toward acne and the study medication.
DRUGBenzoyl peroxide 5% gelTopical benzoyl peroxide 5% gel, to be used once daily to the face.

Timeline

Start date
2009-05-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2010-08-06
Last updated
2018-08-16
Results posted
2011-10-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01176955. Inclusion in this directory is not an endorsement.