# Recruitment of the multiple sclerosis cohort within the European Mobilise-D clinical validation study—lessons learnt, baseline demographics and clinical characteristics

**Authors:** Gavin Brittain, Ellen Buckley, Vita Lanfranchi, Mike Long, Thanos Tsaktanis, Veit Rothhammer, Clint Hansen, Klarissa Hanja Stürner, Walter Maetzler, Lynn Rochester, Lou Sutcliffe, Isabel Neatrour, Beatrix Vereijken, Joren Buekers, Judith Garcia-Aymerich, Sarah Koch, Claudia Armengol, Heiko Gassner, Carl-Philipp Jansen, Daniel Rooks, Letizia Leocani, Giampaolo Brichetto, Gloria Dallas Costa, Clemens Becker, Giancarlo Comi, Basil Sharrack

PMC · DOI: 10.1186/s13063-025-09404-6 · 2026-01-17

## TL;DR

This study describes the recruitment process and baseline characteristics of a multiple sclerosis cohort for a digital mobility assessment study.

## Contribution

The paper provides insights into recruitment challenges and baseline data for a digital mobility study in MS patients.

## Key findings

- 42% recruitment rate with primary sources being clinicians and local registries.
- Participants had a median EDSS score of 5.0 and 58% reported falls in the prior year.
- 556 participants had valid mobility data for analysis.

## Abstract

Multiple sclerosis (MS) is a common cause of disability in working age adults. Current clinical assessments are inadequate at disability assessment or predicting clinically relevant outcomes. Loss of mobility is an important functional disability to people with MS. Mobilise-D aims to develop, validate, and implement a digital mobility solution which measures unsupervised mobility performance across several chronic conditions, including MS, using a single wearable device.

Six hundred two adults with MS, an Expanded Disability Status Scale (EDSS) score of 3.0–6.5, documented disability worsening over the previous 2 years and a 30-day freedom from relapses, were recruited across four European centres.

Of 1416 invited, 602 participants (42%) were recruited. Primary recruitment sources were clinicians (42%) and local registries (42%). Among 616 who declined screening, the main reasons were a lack of interest (44%), the time commitment (25%) or the travel involved (13%). Participants had a mean age of 52 years; 64% were female, with a median EDSS score of 5.0. Of those, 56% had relapsing-remitting MS, 33% secondary progressive MS and 10% primary progressive MS. Falls occurred in 58% of participants in the 12 months prior to recruitment. Of those recruited, 556 (93%) participants had valid mobility data recorded.

The longitudinal collection of clinical and unsupervised mobility assessments will provide a comprehensive dataset, allowing for the determination of digital mobility assessments’ construct validity, predictive capacity, responsiveness, and clinical meaningfulness. Novel insights into real-world mobility that describe both walking activity and gait outcomes will be gained.

The study was registered at the ISRCTN registry on 12/10/2020, titled “Clinical validation of a mobility monitor to measure and predict health outcomes” (ISRCTN Number: 12051706).

The online version contains supplementary material available at 10.1186/s13063-025-09404-6.

## Linked entities

- **Diseases:** Multiple sclerosis (MONDO:0005301)

## Full-text entities

- **Diseases:** infection (MESH:D007239), Impairment of gait (MESH:D020234), Loss of mobility (MESH:D014086), PPMS (MESH:D020528), disability (MESH:D009069), walking limitation (MESH:D013009), Fatigue (MESH:D005221), Comorbidity (MESH:D004194), functional disability (MESH:D003291), RRMS (MESH:D020529), injuries (MESH:D014947), Falls (MESH:C537863), cognitive impairment (MESH:D003072), Corona (MESH:D018352), central nervous system disease (MESH:D002493), fear of falling (MESH:C000719212), anxiety (MESH:D001007), MS (MESH:D009103), pain (MESH:D010146)
- **Chemicals:** alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** 196 del 2021

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12825263/full.md

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Source: https://tomesphere.com/paper/PMC12825263