NCT00518037

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
112

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2006

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2006

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2006

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2006

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

August 15, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 17, 2007

Completed
Last Updated

December 6, 2021

Status Verified

December 1, 2021

Enrollment Period

4 months

First QC Date

August 15, 2007

Last Update Submit

December 2, 2021

Conditions

Nonmelanoma Skin Cancer

Outcome Measures

Primary Outcomes (1)

  • statistics from results of Skindex survey

    1 hour to complete survey

Secondary Outcomes (1)

  • statistics from time-tradeoff utility survey

    1 hour to complete survey

Study Arms (1)

1

nonmelanoma skin cancer patients

Behavioral: surveys

Interventions

surveysBEHAVIORAL

anxiety surveys

1

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

nonmelanoma skin cancer patients

You may qualify if:

  • patients with nonmelanoma skin cancer
  • years of age

You may not qualify if:

  • non-English speakers
  • minors

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Northwestern Memorial Hospital

Chicago, Illinois, 60611, United States

Location

Northwestern University Dermatology

Chicago, Illinois, 60611, United States

Location

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Murad Alam, MD

    Northwestern University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor in Dermatology, Otolaryngology - Head and Neck Surgery and Surgery-Organ Transplantation

Study Record Dates

First Submitted

August 15, 2007

First Posted

August 17, 2007

Study Start

June 1, 2006

Primary Completion

October 1, 2006

Study Completion

October 1, 2006

Last Updated

December 6, 2021

Record last verified: 2021-12

Locations

US(2)