ALS Testing Through Home-based Outcome Measures (ALS AT HOME)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 144
- 试验地点
- 1
- 主要终点
- Adverse Events
研究概览
简要总结
ALS AT HOME is a single-center study of up to 150 participants being done to determine the extent to which frequent sampling can improve the qualities of outcome measures collected at home by study participants.
详细描述
ALS AT HOME is a single-center study of up to 150 participants being done to determine the extent to which frequent sampling can improve the qualities of outcome measures collected at home by study participants.
The objectives of this study are to
- assess the extent to which frequent sampling can reduce variability for the following outcome measures in ALS patients: ALSFRS-R, quantitative hand grip, pulmonary function, EIM in 4 extremities, and actigraphy and voice/speech tracking;
- assess the compliance of ALS patients in obtained outcome measures at home over the course of 9 months;
- directly compare outcome measures collected by patients with measurements obtained at study sites at less frequent intervals by co-enrolling 50 patients participating in the Answer ALS study; and
- provide information to Answer ALS to more fully characterize patients in that study.
The study proposed here will assess the extent to which reducing variability of measurement through frequent sampling can reduce both sample size and duration of clinical trials, provide a first-of-its-kind detailed assessment of disease progression, and evaluate an entirely new paradigm for patient participation in such trials without the need to be geographically yoked to a clinical study center. An important component of this proposal is to jointly recruit 50 patients who also participate in the Answer ALS study that intends to generate 1000 IP cell lines from patients who receive ongoing assessment at 5 clinical sites. The 100 participants that will be co-enrolled in Answer ALS and ALS AT HOME will perform outcome measures at home in addition to having outcome measures performed at clinic sites through Answer ALS participation. Therefore, the investigators will be able to directly assess how the measures obtained by patients at home relate to those obtained by a trained evaluator at a study center using standard metrics. The investigators will also provide all data generated at home to the Answer ALS investigators, further increasing the phenotypic data available for that project.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 85 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •male or female, age 18 to 85 years old,
- •ownership of a Smart Device (phone, tablet, etc) with Bluetooth capabilities,
- •continuous internet access at home,
- •willing and able to provide informed consent in compliance with the regulatory requirements through a web based interface,
- •definite, Probable, or Possible ALS by modified El Escorial criteria, as documented by medical records, with duration from diagnosis 60 months or less, and
- •for the 50 participants in Group 2, participation in the Answer ALS study.
排除标准
- •diagnosed and actively undergoing treatment for cancer, heart failure, end stage renal disease, or another significant medical condition deemed by the PI to likely affect the participant's ability to comply with the protocol,
- •unwilling or unable to comply with the requirements of this protocol, including the presence of any condition (physical, mental, or social) that is likely to affect the participant's ability to comply with the protocol,
- •any other reasons that, in the opinion of the PI, the candidate is determined to be unsuitable for entry into the study.
- •Healthy volunteers who have family members with ALS
结局指标
主要结局
Adverse Events
时间窗: Monthly up to 9 months
Questionnaire
Change in Pulmonary Function
时间窗: Daily for the first 3 months; for the subsequent 6 months measures will be obtained twice weekly
Respirometer
Change in Quantitative Hand Grip
时间窗: Daily for the first 3 months; for the subsequent 6 months measures will be obtained twice weekly
Digital Handgrip Meter
Change in Actigraphy
时间窗: Daily for the first 3 months; for the subsequent 6 months measures will be obtained twice weekly
Activity Band
Change in Electrical Impedance Myography (EIM) Measurements
时间窗: Daily for the first 3 months; for the subsequent 6 months measures will be obtained twice weekly
Skulpt Chisel
ALSFRS-R
时间窗: Weekly up to 9 months
Questionnaire
Change in Voice/Speech Tracking
时间窗: Daily for the first 3 months; for the subsequent 6 months measures will be obtained twice weekly
Smartphone application
Change in Patient-reported Experience measures (PREMs)
时间窗: At Week 1, and then at 3, 6, and 9 months
Questionnaire
次要结局
未报告次要终点
研究者
Jeremy Shefner
Senior Vice President
Barrow Neurological Institute
