Multiple Sclerosis Self Monitoring Study

NCT06125301 | Unknown DMC

• 1 other identifier: NL75687.029.20
• Study Type: interventional
• Target: 225
• Locations: 1 country
• Sites: 1

Brief Summary

This study is a multicenter, prospective, randomized controlled trial (RCT) to compare the effectiveness of a smartphone-based self-monitoring and self-management tool on control self-efficacy with respect to standard clinical practice for patients with relapsing-remitting multiple sclerosis (RRMS). RRMS patients will be recruited and screened for study eligibility at four Dutch MS centers. Following inclusion, participants will be randomly allocated to the intervention group (use of MS sherpa® in addition to standard care) or control group (standard care only). The duration of follow-up is 12 months with study visits at baseline and 12 months, and additional study assessments coupled with every clinical visit as part of standard care during the follow-up period.

Conditions

Multiple Sclerosis

Outcome Measures

Primary Outcomes (1)

• the Multiple Sclerosis Self-Efficacy Control scale (MSSE-C)

  the MS Self-Efficacy scale is an 18-item scale assessing self-rated certainty regarding specific behaviours related to functional independence and psychological management of MS. Items are rated on a scale from 10 (very uncertain) to 100 (very certain). The MSSE consist of two subscales by summing the respective items: SE Function, and SE Control.

  One year

Secondary Outcomes (2)

• Decision making process - caregiver

  One year

• Decision making process - patient

  One year

Study Arms (2)

Intervention group

EXPERIMENTAL

Care as usual + weekly self-monitoring during one year follow-up and discussing app results with caregivers.

Device: MS Sherpa

Control group

NO INTERVENTION

Care as usual.

Interventions

MS Sherpa DEVICE

MS sherpa® is a medical device, intended to support monitoring of persons with MS in order to give patients and their professional healthcare team(s) insight into the presence and progress of symptoms related to MS. MS sherpa® is a system consisting of a smartphone app for data collection and data presentation, a cloud service for data storage, analysis algorithms, and a clinician or research dashboard for user management and data visualization. The device measures the course of symptoms related to MS with respect to walking speed (average walking speed derived from the distance walked during a 2-minute walk), cognitive processing speed, number of correct answers on a smartphone variant of the symbol digit modalities test (SDMT) and patient reported outcomes, through predefined questionnaires regarding fatigue, amongst others. MS sherpa® measures changes in these parameters over time and shows these on an insights screen in the app and on the clinician dashboard.

Intervention group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Signed informed consent form.
• Able to comply with the study protocol, as judged by the investigator.
• A minimum age of 18 years.
• Have a definite diagnosis of RRMS according to the revised McDonald 2017 criteria.
• Have a length of disease duration of ≥12 months, from date of MS diagnosis.
• Have clinical disease activity (one or more reported relapses) and/or radiological disease activity (new/enlarged T2 lesions or T1 contrast-enhancing lesions) within the past 12 months.
• Willing and able to install and use MS sherpa® on own smartphone with Android (version 4.4 or higher) or iOS (version 9 or higher) operating system.
• Willing to stay for treatment with the same hospital during the year of study.
• Willing to follow the rules of conduct as described in Appendix A during the year of study.

You may not qualify if:

• EDSS of \> 6.5 at baseline screening.
• Presence of a cognitive, visual or upper extremity deficit that disables the use or measurements of MS sherpa® on the smartphone, as judged by the investigator.
• Concomitant use of health monitoring apps or devices for MS during the study.
• Concomitant participation in another intervention trial in MS.

Sponsors & Collaborators

• Amsterdam UMC, location VUmc: lead

Study Sites (1)

Amsterdam UMC, locatie VUmc

Amsterdam, Netherlands

RECRUITING

MeSH Terms

Conditions

Multiple Sclerosis

Condition Hierarchy (Ancestors)

Demyelinating Autoimmune Diseases, CNS; Autoimmune Diseases of the Nervous System; Nervous System Diseases; Demyelinating Diseases; Autoimmune Diseases; Immune System Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Prof.

Study Record Dates

• First Submitted: November 28, 2022
• First Posted: November 9, 2023
• Study Start: August 15, 2022
• Primary Completion: August 15, 2024
• Study Completion: August 15, 2024
• Last Updated: November 9, 2023

Record last verified: 2023-11

Data Sharing

• IPD Sharing: Will not share

Locations

NL (1)