Evaluation of the effectiveness of a smartphone app for hay fever treatment assistance in improving subjective symptoms of hay fever.
Not Applicable
- Conditions
- Hay fever
- Registration Number
- JPRN-UMIN000049939
- Lead Sponsor
- Juntendo University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Those who are deemed inappropriate as research subjects by the principal investigator (2) Those who could not give their consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The following items at 4 weeks after the inclusion time point (Day 0) Hay fever subjective symptom assessment: Nasal symptom score (NSS), Non-nasal symptom score (NNSS), Total symptom score (TSS), and Allergic Conjunctival Quality of Life Questionnaire (JACQLQ) Domain II score2
- Secondary Outcome Measures
Name Time Method The following items at 4 weeks after the inclusion time point (Day 0) (1) Basic information on research subjects: age, sex, diagnosis, duration of disease, treatment details (drugs used, duration of treatment) (2) Allergy test results (3) Medication adherence assessment: Medication adherence scale (MMAS-8) (4) Medication record (5) Viewing status of educational contents in the application (6) Operability evaluation