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临床试验/NCT04320381
NCT04320381已完成不适用

Qualitative Understanding of Experiences With the SIMPLIFY Trial

Boston Children's Hospital2 个研究点 分布在 1 个国家目标入组 115 人开始时间: 2020年12月23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
115
试验地点
2
主要终点
Interview #1

研究概览

简要总结

This qualitative longitudinal study is designed to elicit and thematically analyze the perspectives of SIMPLIFY subjects about treatment withdrawal research and treatment burden in the context of triple combination CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) modulator therapy (TCT). Cohorts will be determined based on sub-groups of the assigned treatment arms from the SIMPLIFY study. Participants will be asked to participate in two interviews; the first interview will be conducted at the completion of the SIMPLIFY study and the second interview will be conducted approximately 4 months after the first interview. Trained research staff will conduct the semi-structured interviews that will be audio-recorded and transcribed for thematic analysis. Each interview should last between 30-60 minutes.

详细描述

The recommended daily treatment regimen for CF is complex and results in high treatment burden for many people with CF (PwCF). Newly developed triple combination CFTR modulator therapy (TCT) has shown dramatic health benefits on top of standard CF therapies in a pivotal clinical trial and will soon be a treatment option for a larger population of PwCF. Widespread implementation of TCT will provide an unprecedented opportunity to rigorously study whether PwCF can safely discontinue some previously prescribed daily therapies. The randomized, open-label SIMPLIFY study has been designed to test the hypothesis that withdrawal of dornase alpha and/or nebulized hypertonic saline (HS) is not inferior to continuation of one or both treatments with respect to short-term change in lung function. As this is the first of its kind study design in CF, it unknown how people with CF thinking about withdrawal studies or discontinuing treatments.

Here, the investigators intend to conduct a qualitative interview study that complements the SIMPLIFY protocol in which the investigators aim to assess the experiences of PwCF participating in a treatment withdrawal study. In particular, the investigators will examine post-hoc the beliefs and opinions of a representative subgroup of SIMPLIFY participants about treatment withdrawal research and perceived treatment burden. This qualitative study will provide the opportunity to learn about behaviors after the SIMPLIFY trial, including restarting vs. continuing to maintain medications, withdrawing other medications or therapies, and how patients and families partner with care teams around these decisions. Through these interviews, the investigators will learn how individuals with CF perceive taking part in a drug withdrawal study and how participants discern treatment assignment.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Patient Participant:
  • Participant was randomized into the SIMPLIFY study
  • Person with CF is ≥ 14 years of age at the time of randomization into SIMPLIFY
  • Is English speaking
  • Participant has provided consent (or assent if applicable) in the SIMPLIFY study to provide contact information and share data from the SIMPLIFY study with the QUEST study team
  • Participant has provided contact information via the QUEST portal
  • Is willing and able to adhere to the study requirements
  • Provides consent (or assent if applicable) for the QUEST study
  • Completed participation in the SIMPLIFY study (i.e. completed through Visit 3 or early withdrawal, if applicable)
  • Caregiver Participant:
  • Lives in the same household as a child with CF who is ≥ 14 years of age but <18 years of age who meets the eligibility requirements for the QUEST study
  • Is English speaking,
  • Is willing and able to adhere to the study requirements
  • Provides consent for the QUEST study

排除标准

  • An individual who meets any of the following criteria will be excluded from participation in this study:
  • Any situation that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data

结局指标

主要结局

Interview #1

时间窗: to be conducted at the time of enrollment (post SIMPLIFY study)

Questions to evaluate (A) attitudes and beliefs regarding participation in a withdrawal study and (B) perceptions of treatment burden in the context of having participated in a withdrawal study.

Interview #2

时间窗: to be conducted 4 months following the date of the first interview

Questions to evaluate pwCF's perceptions of (A) factors that affected the decision to use or not use dornase alfa and/or hypertonic saline post-trial participation and satisfaction with the decision and (B) factors that would affect decision-making about whether to withdraw treatments in the future.

次要结局

  • Change in Participant's Perceptions in Interviews(from day one to approximately month 8)
  • Change in Participant's Decision-making in Interviews(from day one to approximately month 8)
  • Change in Participant's Level of Satisfaction in Interviews(from day one to approximately month 8)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gregory Sawicki

Co-Principal Investigator

Boston Children's Hospital

研究点 (2)

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