Compliance and Usability Study Evaluating RHINIX™ Nasal Filters

University of Aarhus1,073 enrolled

Overview

This study will investigate usability and compliance related to rhinix nasal filters for the treatment of seasonal allergic rhinitis (hay fever) during the natural grass pollen season in Denmark.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

1,073

Conditions

Seasonal Allergic Rhinitis

Interventions

Rhinix Nasal FiltersDEVICE

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Motivated to try a different treatment approach to seasonal allergic rhinitis (documented by answering the call-out by Astma-Allergi Danmark) * Indicates having seasonal allergic rhinitis to grass via online questionnaire * Informed consent (by email acceptance after having received information on the trial) * Assess to internet and email Exclusion Criteria: * Improper fit of the Rhinix™ device

Locations (1)

Aarhus University, School of Public Health, Department of Environmental & Occupational Medicine

Aarhus, Denmark

Outcomes

Primary Outcomes

Week 1 likelihood of continued use of RHINIX after study end.

In week 1: The proportion of subjects that rate that they will definitely or are likely to continue using RHINIX after the study is over given that they have stated that they have tried the device.

Time frame: 1 assessment at the end of the 1st week of use.

Week 2 likelihood of continued use of RHINIX after study end.

In week 2: The proportion of subjects that rate that they will definitely or are likely to continue using RHINIX after the study is over given that they have stated that they have tried the device.

Time frame: 1 assessment at the end of the 2nd week of use.

Secondary Outcomes

Week 1 Satisfaction with RHINIX

In week 1: The proportion of subjects who are completely or somewhat satisfied with RHINIX given that they have used the product.

Time frame: 1 assessment at the end of the 1st week

Week 2 satisfaction with RHINIX

In week 2: The proportion of subjects who are completely or somewhat satisfied with RHINIX given that they have used the product.

Time frame: One assessment at the end of the 2nd week

Week 1: RHINIX Control

In week 1: The proportion of subjects who state that RHINIX has helped "to a very high degree" or "to a high degree" in controlling their hay fever symptoms given that they have used the product

Time frame: One assessment at the end of the 1st week of use

Week 2: RHINIX Control

In week 2: The proportion of subjects who state that RHINIX has helped "to a very high degree" or "to a high degree" in controlling their hay fever symptoms given that they have used the product

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.