- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02235116
Predictors of Patient Attitudes and Barriers to Skin Cancer Screening
July 23, 2020 updated by: Jonsson Comprehensive Cancer Center
This is a cross-sectional survey distributed to a convenience sample of patients in a waiting room of an academic dermatology clinic.
The survey assesses patient experiences with full body skin exams and attitudes towards full body skin exams.
The survey is designed to help investigators better understand how many patients are not getting full body skin exams, why this may be occurring, and what types of interventions may be enacted to increase the number of patients getting full body skin exams.
Study Overview
Study Type
Observational
Enrollment (Actual)
1040
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Los Angeles, California, United States, 90095
- UCLA Dermatology
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
English-speaking patients 18yrs old and older attending the UCLA Dermatology clinics in Santa Monica, California or Westwood, California from June 14 to July 1, 2011
Description
Inclusion Criteria:
- 18 years old or older
- English-speaking
Exclusion Criteria:
- previously completed the survey
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients who responded to the survey
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Number of patients reporting ever having had a full body skin examination
Time Frame: 2 weeks
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Melvin Chiu, MD, University of California, Los Angeles
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2011
Primary Completion (ACTUAL)
July 1, 2011
Study Completion (ACTUAL)
July 1, 2011
Study Registration Dates
First Submitted
September 5, 2014
First Submitted That Met QC Criteria
September 8, 2014
First Posted (ESTIMATE)
September 9, 2014
Study Record Updates
Last Update Posted (ACTUAL)
July 27, 2020
Last Update Submitted That Met QC Criteria
July 23, 2020
Last Verified
September 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11-001705
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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