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Clinical Trials/NCT02031718
NCT02031718
Completed
Not Applicable

Comparison Between Interactive Internet-based Education and Counseling for the Management of Acne With That of Internet-based Education Alone

University of California, Davis1 site in 1 country98 target enrollmentJanuary 2014
ConditionsAcne Vulgaris

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acne Vulgaris
Sponsor
University of California, Davis
Enrollment
98
Locations
1
Primary Endpoint
Acne Lesion Counts (Inflammatory and Non-inflammatory)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study will develop and evaluate the efficacy of an Internet-based education program incorporating virtual coaching. For this study, the virtual coach will consist of online videos aimed at providing acne education and promoting behaviors that support healthy skin. The use of Web-based technologies and virtual coaching in acne-related patient education is novel, and may significantly improve clinical outcomes and quality of life in acne patients. We hypothesize that an interactive Internet-based education and counseling program will be more effective than Internet-based education alone in improving clinical outcomes and quality of life in acne patients.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
July 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of mild to moderate acne vulgaris
  • 13 years of age or older at time of assent, may be men or women.
  • Able read and understand English.
  • Able to hear and see the educational videos.
  • Access to computer with Internet access.
  • Capable of giving informed consent.
  • Not currently using any prescription acne treatment.

Exclusion Criteria

  • Non-English speaking individuals.
  • Self-reported exposure to environmental or chemical comedogenic agents
  • Women with self-reported hyperandrogenism (e.g., PCOS)
  • Women self-reporting current use of any form of specific acne-directed hormonal therapy
  • Men or women with self-reported history of Cushing syndrome or congenital adrenal hyperplasia

Outcomes

Primary Outcomes

Acne Lesion Counts (Inflammatory and Non-inflammatory)

Time Frame: Up to 12 weeks

Secondary Outcomes

  • Dermatology Life Quality Index(Up to 12 weeks)

Study Sites (1)

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