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Patient Satisfaction in Cutaneous Surgery

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ClinicalTrials.gov Identifier: NCT01535963
Recruitment Status : Active, not recruiting
First Posted : February 20, 2012
Last Update Posted : February 8, 2017
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
The primary objective of this study is to measure the overall level of satisfaction in patients after cutaneous surgery in 4 different categories, including the surgeon, facility, procedure and recovery and outcome.

Condition or disease
Skin Cancer

Detailed Description:
Secondary objectives are to identify factors associated with patient satisfaction level and determine the correlation between patient satisfaction and surgeon clinical perception.

Study Design

Study Type : Observational
Actual Enrollment : 354 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Pilot Study of Patient Satisfaction After Cutaneous Surgery
Study Start Date : June 2012
Estimated Primary Completion Date : December 2017
Estimated Study Completion Date : December 2017
Groups and Cohorts

Group/Cohort
cutaneous surgery
Patients undergoing cutaneous surgery


Outcome Measures

Primary Outcome Measures :
  1. Patient rating [ Time Frame: at time of visit ]
    Subjects will rate their satisfaction after cutaneous surgery in 4 different categories using 0-10 visual analog scales. The scale will be ~100 millimeters in length and each response will be given a value in millimeters. In addition, patients will answer an open-ended question about their level of satisfaction. Data will also be compared to previous data from patients after cutaneous surgery in the literature.


Secondary Outcome Measures :
  1. Patient ranking [ Time Frame: at time of visit ]
    Subjects will rank the factors determining satisfaction in order of importance using a ranking system for each aspect of care. In addition, the surgeon will rate their satisfaction level and give their perception on patient satisfaction and communication level using 0-10 visual analog scales


Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Patients undergoing cutaneous surgery
Criteria

Inclusion Criteria:

  • 18-80 years old
  • Is in a self-reported stable health condition
  • English speaking
  • Is willing and has the ability to understand the study, provide informed consent and communicate with the investigator
  • Recommended to have and scheduled for cutaneous surgery
  • Agrees to follow-up at scheduled times

Exclusion Criteria:

  • Unable to speak or read English
  • Did not complete an 8th grade education
  • A history of mental illness
  • Any other disability or condition that would prevent completion of questionnaire
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01535963


Locations
United States, Illinois
Northwestern University Feinberg School of Medicine, Department of Dermatology
Chicago, Illinois, United States, 60611
Sponsors and Collaborators
Northwestern University
Investigators
Principal Investigator: Murad Alam, MD Northwestern University
More Information

Responsible Party: Murad Alam, Professor in Dermatology, Otolaryngology - Head and Neck Surgery, and Surgery-Organ Transplantation, Northwestern University
ClinicalTrials.gov Identifier: NCT01535963     History of Changes
Other Study ID Numbers: STU55818
First Posted: February 20, 2012    Key Record Dates
Last Update Posted: February 8, 2017
Last Verified: February 2017

Additional relevant MeSH terms:
Skin Neoplasms
Neoplasms by Site
Neoplasms
Skin Diseases