ALS Testing Through Home-based Outcome Measures

NCT ID: NCT03016897

Last Updated: 2023-02-08

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 144 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-02-22
• Study Completion Date: 2019-09-30

Brief Summary

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.

Detailed Description

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.

Conditions

Amyotrophic Lateral Sclerosis

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Group 1

Participants enrolled solely in ALS AT HOME Outcome measurement devices will be provided. Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Intervention Type: OTHER

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Group 2

Current participants of the Answer ALS study Outcome measurement devices will be provided. Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Intervention Type: OTHER

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Group 3

Participants without neurological disease (controls) Outcome measurement devices will be provided. Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Intervention Type: OTHER

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Interventions

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Respirometer, Handgrip Meter, Skulpt Chisel, ActigraphyMeter

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• 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.

Exclusion Criteria

• 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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Beth Israel Deaconess Medical Center

OTHER

Sponsor Role: collaborator

Jeremy Shefner

OTHER

Sponsor Role: lead

Responsible Party

Jeremy Shefner

Senior Vice President

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Jeremy Shefner, MD

Role: PRINCIPAL_INVESTIGATOR

Barrow Neurological Institute

Locations

Barrow Neurological Institute

Phoenix, Arizona, United States

Countries

United States

Other Identifiers

BNI_ALS_001

Identifier Type: -

Identifier Source: org_study_id