Performance and Safety of a Digital Tool for Unsupervised Self-assessment of NMOSD

NCT ID: NCT05566769

Last Updated: 2025-04-10

Study Results

Results pending

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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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

103 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-03

Study Completion Date

2026-09-30

Brief Summary

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NMOSDCopilot is a digital tool developed for the self-assessment of Neuromyelitis Optica Spectrum Disorder symptoms that impact patients' functioning and quality of life. It has been co-designed with the help of patient advocacy groups, NMOSD patients and medical experts. It includes a smartphone-based application for patients, connected to a web portal developed for healthcare professionals (HCSPs). The patient application is composed of vision, walking, cognition, and dexterity e-active tests inspired by clinical standards, as well as e-questionnaires. The HCP web portal is a desktop-based software that allows HCPs to access the results generated via the patient application and facilitates remote monitoring of patients' symptoms.

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.

Detailed Description

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Conditions

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Neuromyelitis Optica

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

One group
Primary Study Purpose

OTHER

Blinding Strategy

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

Group Type EXPERIMENTAL

NMOSDCopilot smartphone application

Intervention Type DEVICE

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

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Aged over 18 years old
* 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

* Evidence of neurologic, rheumatologic or psychiatric disorder other than NMOSD, including but not limited to major head trauma, seizures or systemic medical diseases that are likely to affect cognitive, upper limb or lower limb functioning
* 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ad scientiam

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University of Southern California

Los Angeles, California, United States

Site Status RECRUITING

University of California Davis Health

Sacramento, California, United States

Site Status RECRUITING

University of south Florida

Tampa, Florida, United States

Site Status RECRUITING

NorthShore University HealthSystem

Evanston, Illinois, United States

Site Status RECRUITING

Johns Hopkins Outpatient Center (now called Levi Watkins, Jr., M.D., Outpatient Center)

Baltimore, Maryland, United States

Site Status RECRUITING

Massachussets General Hospital

Boston, Massachusetts, United States

Site Status RECRUITING

Washington University in St. Louis

Washington, Missouri, United States

Site Status RECRUITING

CC Lou Ruvo Center for Brain Health

Las Vegas, Nevada, United States

Site Status RECRUITING

University of North Carolina at Chapel Hill

Chapel Hill, North Carolina, United States

Site Status RECRUITING

Oklahoma Medical Research Foundation

Oklahoma City, Oklahoma, United States

Site Status RECRUITING

Hôpital Roger Salengro

Lille, , France

Site Status RECRUITING

CHU Marseille - La Timone

Marseille, , France

Site Status RECRUITING

CHU de Montpellier

Montpellier, , France

Site Status RECRUITING

Hopital Pasteur 2

Nice, , France

Site Status RECRUITING

Hopital La Pitié Salpétrière

Paris, , France

Site Status RECRUITING

CHU Rouen

Rouen, , France

Site Status ACTIVE_NOT_RECRUITING

Hopital de Hautepierre

Strasbourg, , France

Site Status COMPLETED

CHU Toulouse - Hôpital Purpan

Toulouse, , France

Site Status RECRUITING

Universitätsklinikum Carl Gustav Carus

Dresden, , Germany

Site Status RECRUITING

Universitätsklinik Essen

Essen, , Germany

Site Status RECRUITING

University Munich

Munich, , Germany

Site Status RECRUITING

Hopital Rechts der Isar der Technischen Universitat Munchen

Munich, , Germany

Site Status NOT_YET_RECRUITING

Countries

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United States France Germany

Central Contacts

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Dr Levy

Role: CONTACT

617-726-7565

Facility Contacts

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Dr Lilyana Amezcua

Role: primary

323 442-5710

Dr Apperson

Role: primary

800 282 3284

John Ciotti, MD

Role: primary

8133969478

Afif Hentati, MD

Role: primary

+1 847-570-2570

Elias S Sotirchos

Role: primary

410-614-1522

Michael Levy, MD, PhD

Role: primary

(617) 726-7565

Robert T Naismith, MD

Role: primary

314-362-3293

Le Hua, MD

Role: primary

7024836000

Dr Dujmovic

Role: primary

984 974-4401

Gabriel Pardo, MD

Role: primary

(405) 271-6673

Helene Zephir, Pr

Role: primary

03 20 44 59 62

Dr Maarouf

Role: primary

04.91.38.00.00

Pierre Labauge, Pr

Role: primary

04 67 33 94 69

Michael Cohen, Dr

Role: primary

04 92 03 77 77

Elisabeth Maillart, Dr

Role: primary

01 42 17 62 05

Dr Ciron

Role: primary

+33 5 61 77 91 06

Dr Ziemssen

Role: primary

+49 (0) 351 458 7450

Dr Pul

Role: primary

+49 201 / 723- 82382

Dr Havla

Role: primary

+49 89 4400 74781

Achim Berthele, Dr

Role: primary

+49 89 41400

Other Identifiers

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OPTIS

Identifier Type: -

Identifier Source: org_study_id

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