Evaluating the Treatment Experience During Initiation of Subcutaneous Immunoglobulin Replacement (SCIG) Therapy at Home Using Alexa Skill
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 22
- 试验地点
- 1
- 主要终点
- Identify Participant Experience, Including Convenience and Satisfaction, With Alexa Skill
研究概览
简要总结
The main aim of this study is to determine the impact of digital health technology, such as Alexa Skill, used to support the initiation of home-based subcutaneous immunoglobulin (SCIG) treatment, treatment management, and overall participant experience.
详细描述
This is a non-interventional, observational study to identify relevant concepts of SCIG treatment experience, as well as satisfaction regarding Alexa skill-assisted SCIG initiation, infusion, and disease/therapy management.
The study will enroll approximately 36 participants (26 patients/caregivers and 10 healthcare professionals [HCPs]). Participants will be enrolled into following observational Cohorts:
- Adult patients with primary immunodeficiency (PID)
- Caregivers of patients with a self-reported diagnosis of PID
- HCPs who prescribe SCIG for patients with PID
Interviews will be conducted by a trained qualitative research interviewer with patients, caregivers, and HCPs, and self-reported data will be collected.
This trial will be conducted in the United States. The overall duration of the study will be approximately 4 months.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients and caregivers:
- •Adult patient (aged 18 years or older) with PID who recently initiated (within 4 months) or will soon initiate (within 30 days) HyQvia or Cuvitru at home or caregiver (aged 18 years or older) supporting participants (any age) with PID who recently initiated (within 4 months) or will soon initiate (within 30 days) HyQvia or Cuvitru at home.
- •Patient has a self-reported physician diagnosis of PID.
- •Resides in the US or US territories.
- •Can speak and read English fluently.
- •Able to participate in an interview(s).
- •Must have a wireless network (Wi-Fi) at home (cannot be a wireless hotspot).
- •Must have an existing Amazon account.
- •Must be willing to receive an Amazon Echo Show device and connect the device to Wi-Fi.
- •Must have a smartphone and be willing to download and use the Alexa application to access the Alexa Skill test.
- •Additional criteria for patients and caregivers completing qualitative debriefing interviews:
- •Must have at least 2 SCIG infusions (HyQvia or Cuvitru) at a residential home or residential assisted living facility within 6 to12 weeks.
- •Must attest to use of Alexa Skill to support at-home SCIG infusions.
- •Resides in the US or US territories.
- •Must be an immunologist or registered nurse/nurse practitioner.
- •Licensed to practice in the US.
- •Can speak and read English fluently.
- •Able to participate in a debriefing interview.
- •Willing to provide informed consent.
- •Must have a wireless network (Wi-Fi).
- •Must have an existing Amazon account.
- •Must be willing to receive an Amazon Echo Show device and connect the device to Wi-Fi.
- •Must have a smartphone and be willing to download and use the Alexa application to access the Alexa Skill test.
- •Must attest to exploration of Alexa Skill as a support tool for patients and caregivers administering SCIG infusions at home.
- •Exclusion Criteria
- •Patients who were previously on SCIG and transitioned to either HyQvia or Cuvitru SCIG product will be excluded.
排除标准
- 未提供
结局指标
主要结局
Identify Participant Experience, Including Convenience and Satisfaction, With Alexa Skill
时间窗: 4 months
Qualitative interviews with patients, caregivers, and HCPs who will be using the Alexa Skill to support initiation of SCIG for PID to characterize their experience, including convenience and satisfaction. Qualitative interviews will be semi-structured to comprehensively assess confidence and satisfaction, but also open-ended to give patients, families, and HCPs freedom to discuss their experience.
次要结局
未报告次要终点