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Development and Validation of a Quality of Life Instrument for Actinic Keratosis


N/A
18 Years
N/A
Not Enrolling
Both
Actinic Keratosis

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Trial Information

Development and Validation of a Quality of Life Instrument for Actinic Keratosis


Inclusion Criteria:



- Male or female, age 18 years or older being seen in a dermatology clinic

- Informed consent of participation must be given by subject

Exclusion Criteria:

- Inability to complete all study questionnaires.

- Subjects who are unable to read and write English

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label

Outcome Measure:

Difference in questionnaire score in patients with Actinic keratosis and with out actinic keratosis

Outcome Description:

We are developing an actinic keratosis risk assessment questionnaire and is designed to distinguish patients who have a higher likelihood of having a diagnosis of actinic keratosis. The outcome measure is the difference in scores between those with actinic keratosis and those without.

Outcome Time Frame:

Baseline

Safety Issue:

No

Principal Investigator

Steven R Feldman, MD, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Wake Forest University

Authority:

United States: Institutional Review Board

Study ID:

00017619

NCT ID:

NCT01444989

Start Date:

September 2011

Completion Date:

March 2012

Related Keywords:

  • Actinic Keratosis
  • "Sun spots"
  • "Pre-cancerous skin lesion"
  • Keratosis
  • Keratosis, Actinic

Name

Location

Wake Forest Health Sciences DermatologyWinston Salem, North Carolina  27104