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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00518037
Other study ID # 1253-006
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2006
Est. completion date October 2006

Study information

Verified date December 2021
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study is to learn more about the physical discomfort, sensory impairment, depression, anxiety, and interference with relationships, family, and work associated with NMSC via survey questions.


Description:

The purpose of this study is to learn more about the physical discomfort, sensory impairment, depression, anxiety, and interference with relationships, family, and work associated with NMSC via survey questions.


Recruitment information / eligibility

Status Completed
Enrollment 112
Est. completion date October 2006
Est. primary completion date October 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - patients with nonmelanoma skin cancer - 18 years of age Exclusion Criteria: - non-English speakers - minors

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
surveys
anxiety surveys

Locations

Country Name City State
United States Northwestern Memorial Hospital Chicago Illinois
United States Northwestern University Dermatology Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary statistics from results of Skindex survey 1 hour to complete survey
Secondary statistics from time-tradeoff utility survey 1 hour to complete survey
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