3.8 Article

Neuropsychological evaluation and rehabilitation in multiple sclerosis (NEuRoMS): protocol for a mixed-methods, multicentre feasibility randomised controlled trial

Journal

PILOT AND FEASIBILITY STUDIES
Volume 8, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s40814-022-01073-5

Keywords

Multiple sclerosis; Cognition; Cognitive screening; Rehabilitation; Feasibility study; Randomised controlled trial

Funding

  1. National Institute for Health and Care Research [RP-PG-0218-20002]
  2. National Institutes of Health Research (NIHR) [RP-PG-0218-20002] Funding Source: National Institutes of Health Research (NIHR)

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This study aims to develop a cognitive screening and management pathway for people with multiple sclerosis (MS) and evaluate its feasibility. Through observational study, a feasibility randomized controlled trial, and semi-structured interviews, researchers will assess the clinical and cost-effectiveness of the intervention as well as its potential impact on the management of cognitive problems in MS patients.
Background: Cognitive problems affect up to 70% of people with multiple sclerosis (MS), which can negatively impact mood, ability to work, and quality of life. Addressing cognitive problems is a top 10 research priority for people with MS. Our ongoing research has systematically developed a cognitive screening and management pathway (NEuRoMS) tailored for people with MS, involving a brief cognitive evaluation and rehabilitation intervention. The present study aims to assess the feasibility of delivering the pathway and will inform the design of a definitive randomised controlled trial (RCT) to investigate the clinical and cost-effectiveness of the intervention and eventually guide its clinical implementation. Methods: The feasibility study is in three parts. Part 1 involves an observational study of those who receive screening and support for cognitive problems, using routinely collected clinical data. Part 2 is a two-arm, parallel group, multicentre, feasibility RCT with a nested fidelity evaluation. This part will evaluate the feasibility of undertaking a definitive trial comparing the NEuRoMS intervention plus usual care to usual care only, amongst people with MS with mild cognitive problems (n = 60). In part 3, semi-structured interviews will be undertaken with participants from part 2 (n = 25), clinicians (n = 9), and intervention providers (n = 3) involved in delivering the NEuRoMS cognitive screening and management pathway. MS participants will be recruited from outpatient clinics at three UK National Health Service hospitals. Discussion: Timely screening and effective management of cognitive problems in MS are urgently needed due to the detrimental consequences of cognitive problems on people with MS, the healthcare system, and wider society. The NEuRoMS intervention is based on previous and extant literature and has been co-constructed with relevant stakeholders. If effective, the NEuRoMS pathway will facilitate timely identification and management of cognitive problems in people with MS.

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