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Analysis of Adherence in Subjects Undergoing Differin Gel, 0.1% Treatment of Moderate to Severe Acne Vulgaris

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Steven R. Feldman, Wake Forest University Health Sciences
ClinicalTrials.gov Identifier:
NCT00696449
First received: June 9, 2008
Last updated: February 10, 2017
Last verified: February 2017

June 9, 2008
February 10, 2017
June 2006
May 2007   (Final data collection date for primary outcome measure)
Adherence to Treatment [ Time Frame: 12 weeks ]
Percentage of prescribed doses taken over the 12-week study period, as measured by a Medication Event Monitoring System (MEMS) cap
Percent change from baseline in total lesions counts [ Time Frame: 12 weeks ]
Complete list of historical versions of study NCT00696449 on ClinicalTrials.gov Archive Site
Not Provided
Global Assessment of improvement from baseline. [ Time Frame: 12 weeks ]
Not Provided
Not Provided
 
Analysis of Adherence in Subjects Undergoing Differin Gel, 0.1% Treatment of Moderate to Severe Acne Vulgaris
An Analysis of Adherence and Associated Factors in Subjects Undergoing Differin Gel, 0.1% Treatment of Moderate to Severe Acne Vulgaris
The primary objective of this study is to investigate potential differences between four treatment intervention groups in the adherence to treatment with Differin® Gel, 0.1%. Differin is approved by the Food and Drug Administration (FDA) to treat acne.

Subjects will be enrolled and randomized in a 1:1:1:1 ratio to one of four treatment intervention groups. All Subjects will be treated once-daily for 12 weeks with Differin® Gel, 0.1%. The four intervention groups were designated according to follow-up strategies as follows:

  • More frequent than normal office visits
  • Electronic reminders (voice, e-mail, text messages)
  • Parental involvement/intervention reminders
  • No intervention or reminders
Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Investigator
Primary Purpose: Treatment
Acne Vulgaris
  • Drug: Adapalene
    All Subjects will treat the face once daily in the evening.
    Other Name: Differin® Gel, 0.1%
  • Behavioral: frequent visits
    This group will be asked to return to the study center on weeks 1, 2, 4 and 8 for office visits (to remind the Subject to apply the study medication); in addition to the study visits on Weeks 6 and 12.
  • Behavioral: electronic reminder
    This group will receive a daily electronic reminder by email, text pager, or phone message (approximately at the same time each day) to use the study medication within a 4-hour window after the reminder and will return to the study center for study visits on Weeks 6 and 12.
  • Behavioral: Parent reminder
    In this group parents will be prompted by a daily electronic message by email, text pager, or phone message (approximately at the same time each day) to remind the Subject to use the study medication within a 4-hour window after the reminder. Parents will be instructed to then verbally deliver the message to the study Subject. Subjects will return to the study center for study visits on Weeks 6 and 12.
  • Behavioral: Standard of care
    This group is considered to be the "standard of care" arm and will return to the study center for study visits on Weeks 6 and 12. This group will not receive any kind of reminders other than the instructions provided by the study staff during the study visits.
  • Experimental: Frequent visits
    This group will be asked to return to the study center on weeks 1, 2, 4 and 8 for office visits (to remind the Subject to apply the study medication); in addition to the study visits on Weeks 6 and 12.
    Interventions:
    • Drug: Adapalene
    • Behavioral: frequent visits
  • Experimental: Electronic reminder
    This group will receive a daily electronic reminder by email, text pager, or phone message (approximately at the same time each day) to use the study medication within a 4-hour window after the reminder and will return to the study center for study visits on Weeks 6 and 12.
    Interventions:
    • Drug: Adapalene
    • Behavioral: electronic reminder
  • Experimental: Parent reminder
    In this group parents will be prompted by a daily electronic message by email, text pager, or phone message (approximately at the same time each day) to remind the Subject to use the study medication within a 4-hour window after the reminder. Parents will be instructed to then verbally deliver the message to the study Subject. Subjects will return to the study center for study visits on Weeks 6 and 12.
    Interventions:
    • Drug: Adapalene
    • Behavioral: Parent reminder
  • Experimental: Standard of care
    This group is considered to be the "standard of care" arm and will return to the study center for study visits on Weeks 6 and 12. This group will not receive any kind of reminders other than the instructions provided by the study staff during the study visits.
    Interventions:
    • Drug: Adapalene
    • Behavioral: Standard of care
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
61
October 2009
May 2007   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or female Subjects of any race, aged 13 to 18 years inclusive,
  • Subjects with a diagnosis of moderate to severe Acne vulgaris, measured by lesion counts of a minimum of 15 and a maximum of 50 inflammatory lesions (papules and pustules) on the face, AND a minimum of 30 and a maximum of 125 total lesions. Subjects with nodules may participate in the study.
  • Female Subjects of childbearing potential must have a negative urine pregnancy test (UPT).
  • Female Subjects of childbearing potential must practice a highly effective method of contraception during the study
  • Subjects (and parent/guardian if Subject is under 18 years of age) must be willing and capable of following study instructions to the extent and degree required by the protocol;
  • Subjects able to follow study instructions and likely to complete all required visits;
  • Subjects/Representative signs the Informed Consent prior to any study procedures. Subjects under the age of 18 must have one parent or guardian read and sign the Informed Assent Form prior to receiving study treatment but the parent(s) or guardian is not required to attend the follow-up visits unless requested;
  • Subject must be willing to be photographed and sign a release form allowing photographs to be used.

Exclusion Criteria:

  • Female Subjects who are pregnant, nursing or planning a pregnancy during the study,
  • Subjects with a condition or who are in a situation which, in the Investigator's opinion, may put the Subject at risk, may confound the study results, or may interfere with the Subject's participation in the study,
  • Subjects with known allergy to one of the components of the test products,
  • Subjects who have participated in another investigational drug or device research study within 30 days of enrolment, Subjects with acne conglobata, acne fulminans, secondary acne (chloracne, drug-induced acne, etc.), or or severe acne requiring more than topical treatment (e.g. oral isotretinoin);
  • Subjects with a beard or other facial hair that might interfere with study assessments;
  • Subjects with underlying diseases or other dermatological conditions that require the use of interfering topical or systemic therapy such as, but not limited to, atopic dermatitis, perioral dermatitis or rosacea;
  • Subjects who are at risk in terms of precautions, warnings, and contra-indication (see package insert for Differin Gel, 0.1%);
  • Subjects who foresee intensive UV exposure during the study (mountain sports, UV radiation, sunbathing, etc.);
  • Subjects with a known history of drug and/or alcohol abuse.
Sexes Eligible for Study: All
13 Years to 18 Years   (Child, Adult)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00696449
00000406
31219
No
Not Provided
No
Not Provided
Steven R. Feldman, Wake Forest University Health Sciences
Wake Forest University
Not Provided
Principal Investigator: Steve Feldman, MD, PhD Wake Forest University Health Sciences
Wake Forest University Health Sciences
February 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP