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Legionnaires' Effect on Smell

Completed
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
Inclusion Criteria
  • 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.
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Exclusion Criteria
  • Age less than 18
  • Pregnant Women
  • Persons who mental competence is limited, such as those with dementia
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Legionnaires' Disease VolunteersThe University of Pennsylvania Smell Identification Test (UPSIT)Volunteers who have been diagnosed/survivors of Legionnaire's Disease
Healthy VolunteersThe University of Pennsylvania Smell Identification Test (UPSIT)Volunteers who are healthy.
Primary Outcome Measures
NameTimeMethod
Score on the University of Pennsylvania Smell Identification Test20-30 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
NameTimeMethod
Questionnaire Responses20-30 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

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