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临床试验/NCT05146206
NCT05146206已完成不适用

Patient Satisfaction and Sensory Attributes of Nasal Spray Treatments for Allergic Rhinitis

Community and Patient Preference Research Pty Ltd1 个研究点 分布在 1 个国家目标入组 426 人开始时间: 2021年11月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
426
试验地点
1
主要终点
Overall Best-Worst Scaling Task Index Score (Treatment Satisfaction Index Score)

研究概览

简要总结

The study seeks to understand patients' satisfaction and importance of treatment attributes for Allergic Rhinitis nasal sprays from two brands (RYALTRIS® vs. DYMISTA®).

详细描述

The study seeks to understand patients' satisfaction and importance of treatment attributes for Allergic Rhinitis nasal sprays from two brands (RYALTRIS® vs. DYMISTA®).

To directly compare patient satisfaction with 2 different Allergic Rhinitis nasal sprays, an observational, cross-sectional study design with 2 independent samples was chosen. Participants will complete an online survey involving a Best-Worst scaling (BWS) task to determine satisfaction and importance index for sensory attributes.

The suggested treatment attributes are informed by a range of previous studies, including those conducted by Meltzer et al 2005 and Price et al 2020, and methodology from CaPPRe's own work in developing indices for importance and satisfaction of treatment attributes using BWS.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Allergic Rhinitis patients (moderate-to-severe Seasonal Allergic Rhinitis or Perennial Allergic Rhinitis) with or without conjunctivitis who meet the following criteria will be offered the opportunity to participate in the study:
  • Patients above 18 years old
  • Fluent in English
  • Patients initiated on RYALTRIS® or DYMISTA® nasal spray in the last 12 months and currently using treatment
  • Willing and able to provide consent to participate

排除标准

  • Have reported a loss of taste and/or smell related to COVID-19 (or other medical condition)
  • Are employed by a pharmaceutical company (to avoid conflict of interest)
  • Are employed by a vaccine company (to avoid conflict of interest)
  • Do not have access to the internet (to ensure validity of the data)
  • Are unable to read and understand English (to ensure validity of the data)

结局指标

主要结局

Overall Best-Worst Scaling Task Index Score (Treatment Satisfaction Index Score)

时间窗: Cross-sectional - through study completion, an average of 3 months

The primary study endpoint is the overall index score from the Best Worst Scaling exercise, to reflect satisfaction and importance of treatment attributes of the RYALTRIS® and DYMISTA® nasal spray. Index scores from the Best Worst Scaling exercise range from 0 to 100, with higher scores indicating higher satisfaction of treatment attributes.

次要结局

  • Rescaled Scores From Best-Worst Scaling Task(Cross-sectional - through study completion, an average of 3 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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