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临床试验/NCT03016897
NCT03016897已完成不适用

ALS Testing Through Home-based Outcome Measures (ALS AT HOME)

Jeremy Shefner1 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2017年2月22日最近更新:
适应症

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

  1. 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;
  2. assess the compliance of ALS patients in obtained outcome measures at home over the course of 9 months;
  3. 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
  4. 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

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

发起方
Jeremy Shefner
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jeremy Shefner

Senior Vice President

Barrow Neurological Institute

研究点 (1)

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