Feasibility of Measuring Skin Carotenoid Level in an Asthma Clinic
- 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
- 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
- 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
Name Time Method FEV1 measured 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
ACT measured 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 Level measured 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 Intake measured 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
Name Time Method
Trial Locations
- Locations (1)
University of Kansas Medical Center
🇺🇸Kansas City, Kansas, United States