Validation of a Dermatology-Specific Treatment Satisfaction Instrument
1 other identifier
observational
120
1 country
1
Brief Summary
The primary objective of this study is to validate a dermatology-specific questionnaire that assesses patient satisfaction with their treatments across various inflammatory dermatology diseases.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2021
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 14, 2021
CompletedFirst Posted
Study publicly available on registry
September 24, 2021
CompletedStudy Start
First participant enrolled
November 13, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 14, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2023
CompletedNovember 15, 2023
November 1, 2023
1.3 years
September 14, 2021
November 14, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Validity and reliability of a dermatology-specific treatment satisfaction instrument in patients with psoriasis
For this survey study, the investigators will gather descriptive statistics for each item in the questionnaire. The investigators will also measure the following psychometric properties: measurement error, reliability and construct validity, as measured by convergent and known-groups validity
8 months
Interventions
Study subjects will also be administered a dermatology-specific treatment satisfaction questionnaire, as well as other questionnaires including the generic validated Treatment Satisfaction Questionnaire for Medication (TSQM-9) and the validated Dermatology Life Quality Index (DLQI). Study participants will also self-report their disease severity using PGA. Depending on patients' preferred method of interacting with the study team, the investigators will collect their responses to these questionnaires either in-person, over the phone, or electronically via secure research platforms.
Eligibility Criteria
Adult (≥ 18 years) dermatology patients with psoriasis from LAC+USC and Keck Medical Centers, the Brigham and Women's Hospital, and the Mount Sinai Hospital.
You may qualify if:
- Adult (≥ 18 years)
- Psoriasis patients undergoing some form of treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Southern Californialead
- Icahn School of Medicine at Mount Sinaicollaborator
- Brigham and Women's Hospitalcollaborator
Study Sites (1)
University of Southern California
Los Angeles, California, 90089, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
April Armstrong, MD, MPH
University of Southern California
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
September 14, 2021
First Posted
September 24, 2021
Study Start
November 13, 2021
Primary Completion
March 14, 2023
Study Completion
December 1, 2023
Last Updated
November 15, 2023
Record last verified: 2023-11