Quality of Life in Patients With Nonmelanoma Skin Cancer

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.

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Key information

Conditions

Nonmelanoma Skin Cancer

Sex eligibility

All sexes

Study type

Observational

Primary location

Northwestern Memorial Hospital, Chicago, Illinois, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

patients with nonmelanoma skin cancer
18 years of age

Exclusion criteria

non-English speakers
minors

Treatment and study plan

Surveys

Behavioral

anxiety surveys

Primary outcomes

statistics from results of Skindex survey

Time frame: 1 hour to complete survey

Secondary outcomes

statistics from time-tradeoff utility survey

Time frame: 1 hour to complete survey

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Registry information

Important dates

Study start: 2006
Primary completion: 2006
Study completion: 2006
First posted: Aug 17, 2007
Registry last updated: Dec 6, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed