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临床试验/NCT03315572
NCT03315572已完成不适用

Qualitative Research to Support Ellipta Ease-of-Use Questions in Pediatric Patients With Asthma

GlaxoSmithKline1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2017年10月17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
28
试验地点
1
主要终点
Number of Pediatric Participants With Difficulty in Distinguishing Between the Item Responses-Round 1 Interviews

研究概览

简要总结

A range of devices has been developed to administer inhaled therapy for asthma, including dry powder inhaler (DPI) devices. ELLIPTA is a DPI that is preloaded with a drug therapy to treat asthmatic subjects. The objective of this study is to revise ease of use items developed for adults to be appropriate for completion by pediatric subjects in future clinical trials and to evaluate the newly developed items in subjects with asthma aged 5 to 11 years and their caregivers. This is a cross-sectional, qualitative study that will involve pediatric subjects with asthma who are currently using an asthma maintenance inhaler and their caregivers. Two rounds of repetitive cognitive interviews will be conducted with 16 subjects in each interview set. Each interview will last approximately 45 minutes. Data provided by pediatric subjects and their caregivers during interview will be collected as field notes and audio recordings which will be transcribed.

研究设计

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

入排标准

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

入选标准

  • Child inclusion criteria
  • Be 5 to 11 years of age
  • Have asthma
  • Currently use a maintenance inhaler to treat their asthma
  • Be willing and able to provide assent
  • Be willing and able to participate in a 45-minute interview in English Caregiver inclusion criteria
  • Above 18+ years of age
  • Be a caregiver (parent or legal guardian) of a pediatric subject with asthma that meets the criteria above
  • Be willing and able to provide signed and dated informed consent and parental permission in English
  • Be willing and able to participate in a 45-minute interview

排除标准

  • 未提供

结局指标

主要结局

Number of Pediatric Participants With Difficulty in Distinguishing Between the Item Responses-Round 1 Interviews

时间窗: Up to 45 minutes

Round 1 of the interviews evaluated 3 items to evaluate ease of use of inhaler (Items 1a, 1b and 1c), 3 items to assess the ease in evaluating remaining doses (Items 2a, 2b, 2c) and one item to understand if the participants could compare different types of inhalers. Three response options were developed to assess ease of inhaler use and ease of evaluating remaining doses: Item 1a/2a-a verbal response scale with four options (Very easy, easy, hard, very hard); Item 1b/2b-the same four verbal response options accompanied by illustrations of faces for each verbal response; and Item 1c/2c-a verbal response scale with two options (Yes, No). Item 3 consisted of 3 response options (Yes, No, The same). The number of participants who had difficulty in distinguishing item responses has been presented.

Number of Pediatric Participants With Problems Understanding Item Wording-Round 2 Interviews

时间窗: Up to 45 minutes

Based on the results of Round 1 interviews, the four level verbal response scale (Item 1a and Item 2a) of the pediatric versions were selected for further evaluation of ease of use and ease in evaluating remaining doses in Round 2. The second set of interviews were conducted to test if any further revision is required to optimize the items. The items for evaluation in Round 2 included: Item 1 and Item 2 for ease of ELLIPTA use and ease of evaluating remaining doses with a verbal scale of four options (Very easy, Easy, Hard, Very hard) and Item 3 for evaluation of the ability of participants to differentiate between inhalers consisting of three options (Yes, No, The same). The number of pediatric participants with problems understanding item wording has been presented.

Number of Pediatric Participants With Difficulty Providing Responses to Items-Round 2 Interviews

时间窗: Up to 45 minutes

The items for evaluation in Round 2 included: Item 1 and Item 2 for ease of ELLIPTA use and ease of evaluating remaining doses with a verbal scale of four options (Very easy, Easy, Hard, Very hard) and Item 3 for evaluation of the ability of participants to differentiate between inhalers consisting of three options (Yes, No, The same). The number of pediatric participants with difficulty in providing response to items has been presented.

Number of Pediatric Participants With Problems Understanding Item Wording-Round 1 Interviews

时间窗: Up to 45 minutes

The items for pediatric participants were developed to assess the concepts of overall ease of use of ELLIPTA and ease of evaluating remaining doses in inhaler. Pediatric participants aged 5 to 7 years were required to complete the interviewer-administered version and participants aged 8 to 11 years were administered self-completed version. Round 1 of the interviews evaluated 3 items to evaluate ease of use of inhaler (Items 1a, 1b and 1c), 3 items to assess the ease in evaluating remaining doses (Items 2a, 2b, 2c) and one item to assess if the pediatric participants could compare different types of inhalers (Item 3). The number of participants who had problems in understanding the item wordings has been presented. No statistical analyses were conducted for this qualitative study.

Number of Pediatric Participants With Difficulty Providing Responses to Items-Round 1 Interviews

时间窗: Up to 45 minutes

Round 1 of the interviews evaluated 3 items to evaluate ease of use of inhaler (Items 1a, 1b and 1c) and 3 items to assess the ease in evaluating remaining doses (Items 2a, 2b, 2c). Three response options were developed for these two concepts: Item 1a/2a-a verbal response scale with four options (Very easy, easy, hard, very hard); Item 1b/2b-the same four verbal response options accompanied by illustrations of faces for each verbal response; and Item 1c/2c-a verbal response scale with two options (Yes, No). The number of participants who had difficulty in providing item responses has been presented.

Number of Caregiver Participants Who Had Difficulty Providing Responses to Caregiver Items-Round 1 Interviews

时间窗: Up to 45 minutes

Round 1 of the interviews for caregiver participants evaluated the concepts of ease of evaluating remaining doses (Item 1) and the likelihood of requesting inhaler from their child's physician (Item 2). A response scale with four options was developed for each item: Item 1 (Very easy, Easy, Difficult, Very difficult) and Item 2 (Very likely, Likely, Unlikely, Very unlikely). The number of caregivers who had difficulty in providing responses to caregiver items has been reported.

Number of Caregiver Participants Who Had Difficulty Providing Responses to Caregiver Items-Round 2 Interviews

时间窗: Up to 45 minutes

Based on the results of Round 1 interviews, both the items of caregiver version were retained for further evaluation in Round 2. The number of caregivers who had difficulty in providing responses to caregiver version of items has been presented below.

Number of Additional Ease of Use Items Identified

时间窗: Up to 45 minutes

Caregivers were asked if there were any concepts regarding ease of use that were missing from the pediatric or caregiver versions according to them. The number of ease of use items as identified by caregiver participants has been presented.

Number of Pediatric Participants With Difficulty in Distinguishing Between the Responses to Items-Round 2 Interviews

时间窗: Up to 45 minutes

The items for evaluation in Round 2 included: Item 1 and Item 2 for ease of ELLIPTA use and ease of evaluating remaining doses with a verbal scale of four options (Very easy, Easy, Hard, Very hard) and Item 3 for evaluation of the ability of participants to differentiate between inhalers consisting of three options (Yes, No, The same). The number of pediatric participants who had difficulty in distinguishing between the response to items has been presented.

次要结局

  • Number of Pediatric Participants Who Were Able to Use ELLIPTA Whistle(Up to 45 minutes)
  • Number of Participants With Attempts Required to Produce an Audible Sound(Up to 45 minutes)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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