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Feasibility of Measuring Skin Carotenoid Level in an Asthma Clinic

Completed
Conditions
Asthma
Registration Number
NCT06636396
Lead Sponsor
University of Kansas Medical Center
Brief Summary

The purpose of this study is to assess the use of a practical tool to objectively measure the fruit and vegetable intake in people with asthma.

Detailed Description

After consenting to join the study, all participants enter a single cohort, cross-sectional study to assess pulmonary function, asthma control, carotenoid level, and diet intake.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
29
Inclusion Criteria
  • Pulmonary patients 18 years of age and older
  • Confirmed diagnosis of asthma by a physician and confirmed by a pulmonary physician
  • English speaking
  • Access to the internet
Exclusion Criteria
  • Acute upper or lower respiratory infection
  • Systemic corticosteroids
  • Recent or current confirmed diagnosis of Covid-19

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
FEV1measured at a single time point when recruited in the study (cross sectional). Study outcomes will be reported upon study completion, approximately 1 year from study onset.

forced expiratory volume in one second

ACTmeasured at a single time point when recruited in the study (cross sectional). Study outcomes will be reported upon study completion, approximately 1 year from study onset.

Asthma control test results in a score of 5-25, with a lower score indicating better asthma control.

Skin Carotenoid Levelmeasured at a single time point when recruited in the study (cross sectional). Study outcomes will be reported upon study completion, approximately 1 year from study onset.

Skin carotenoid level, measured with a non-invasive tool and is an indicator of fruit and vegetable intake. Skin carotenoid levels are shown as a score of 0-800, with a higher score representing a higher level of carotenoids.

Diet Intakemeasured at a single time point when recruited in the study (cross sectional). Study outcomes will be reported upon study completion, approximately 1 year from study onset.

Nutrascreen diet questionnaire to assess nutritional intake. Specifically, quantity of fruits and vegetable intake will be assessed.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Kansas Medical Center

🇺🇸

Kansas City, Kansas, United States

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