Legionnaires' Effect on Smell
- Conditions
- Legionnaires' Disease
- Interventions
- Other: The University of Pennsylvania Smell Identification Test (UPSIT)
- Registration Number
- NCT03321786
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
The goal of this study is to determine whether survivors of Legionnaires' disease suffer smell loss. A quantitative olfactory test will be performed by the participants. Such testing will require approximately 20-30 minutes of the participant's time. The participants will take the University of Pennsylvania Smell Identification Test (UPSIT), a scratch-and-sniff test to assess their ability to identify odors in a forced- choice format. Volunteers will also complete a questionnaire asking personal history, demographic questions, and medical history.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 10
- Persons of generally good health, as obtained from a screening questionnaire who are 18 years of age and older
- Both men and women of all ethnic backgrounds will be accepted.
- Age less than 18
- Pregnant Women
- Persons who mental competence is limited, such as those with dementia
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Legionnaires' Disease Volunteers The University of Pennsylvania Smell Identification Test (UPSIT) Volunteers who have been diagnosed/survivors of Legionnaire's Disease Healthy Volunteers The University of Pennsylvania Smell Identification Test (UPSIT) Volunteers who are healthy.
- Primary Outcome Measures
Name Time Method Score on the University of Pennsylvania Smell Identification Test 20-30 Minutes The number of correct odor identification responses out of 40 from the standardized University of Pennsylvania Smell Identification Test.
The total number of correct responses will then be compared to standard norms of correct responses based on demographic information such as age and sex. Comparing the scores to the standard norms collected will indicate whether a volunteer is normosmic, hyposmic, or anosmic.
- Secondary Outcome Measures
Name Time Method Questionnaire Responses 20-30 Minutes These are various demographic and medical history questions regarding exposure to Legionella Pneumonia and current experiences post diagnosis and treatment.
Trial Locations
- Locations (1)
University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States