Performance and Safety of a Digital Tool for Unsupervised Self-assessment of NMOSD
NCT ID: NCT05566769
Last Updated: 2025-04-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
103 participants
INTERVENTIONAL
2023-11-03
2026-09-30
Brief Summary
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The objectives of this study are to validate the accuracy, reliability and reproducibility of the unsupervised at-home self-assessment of symptoms on the patient's smartphone versus the standard in-clinic testing, as well as to evaluate the safety of use of the tool, its usability, and satisfaction towards the patient application among NMOSD patients, and the HCP web dashboard among HCPs.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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NMOSDCopilot
Performance of digital tests and standard test in clinic at D0 and M6 Use of NMOSDCopilot at-home in between visits during 12 months
NMOSDCopilot smartphone application
NMOSDCopilot includes active tests for walking, cognition, dexterity and vision, and e-questionnaires related to pain, fatigue, quality of life, bladder and bowel dysfunction, depression
Interventions
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NMOSDCopilot smartphone application
NMOSDCopilot includes active tests for walking, cognition, dexterity and vision, and e-questionnaires related to pain, fatigue, quality of life, bladder and bowel dysfunction, depression
Eligibility Criteria
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Inclusion Criteria
* NMOSD as defined by the 2015 international consensus diagnostic criteria (AQP4+ only)
* With NMOSD treatment (treatment must be unchanged since 6 months before enrollment, and 1 month for analgesics, antidepressants, neuroleptics)
* EDSS =\< 7
* With no evidence of relapse in the past 3 months before enrollment
* Who have read the information sheet and signed the informed consent form
* Able to use a smartphone
* Owns a personal smartphone which version is above 13 for IOS and 8 for Android included
* Able to read language in which the mobile application is available and able to understand pictograms
Exclusion Criteria
* Pregnant and nursing women
* Person under guardianship or curatorship
* Bedridden patients or patients with a daily activity of less than 2 hours per day
* Current drugs or/and alcohol abuse that could influence performance on the tests (clinician's judgment)
* Subject has participated in another clinical study within the previous 30 days of screening or is currently participating in another study that, in the opinion of the Investigator, might interfere with the participant's full participation in the study or confound the assessment of the participant or outcome of the study.
18 Years
ALL
No
Sponsors
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Ad scientiam
OTHER
Responsible Party
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Locations
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University of Southern California
Los Angeles, California, United States
University of California Davis Health
Sacramento, California, United States
University of south Florida
Tampa, Florida, United States
NorthShore University HealthSystem
Evanston, Illinois, United States
Johns Hopkins Outpatient Center (now called Levi Watkins, Jr., M.D., Outpatient Center)
Baltimore, Maryland, United States
Massachussets General Hospital
Boston, Massachusetts, United States
Washington University in St. Louis
Washington, Missouri, United States
CC Lou Ruvo Center for Brain Health
Las Vegas, Nevada, United States
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, United States
Oklahoma Medical Research Foundation
Oklahoma City, Oklahoma, United States
Hôpital Roger Salengro
Lille, , France
CHU Marseille - La Timone
Marseille, , France
CHU de Montpellier
Montpellier, , France
Hopital Pasteur 2
Nice, , France
Hopital La Pitié Salpétrière
Paris, , France
CHU Rouen
Rouen, , France
Hopital de Hautepierre
Strasbourg, , France
CHU Toulouse - Hôpital Purpan
Toulouse, , France
Universitätsklinikum Carl Gustav Carus
Dresden, , Germany
Universitätsklinik Essen
Essen, , Germany
University Munich
Munich, , Germany
Hopital Rechts der Isar der Technischen Universitat Munchen
Munich, , Germany
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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OPTIS
Identifier Type: -
Identifier Source: org_study_id
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