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Feasibility of a Vocational Rehabilitation Intervention for Job Retention in Workers With MS-RiaLSM Intervention Project

Development and Assessment of a Vocational Rehabilitation Intervention for Job Retention in Workers With Multiple Sclerosis (RiaLSM Intervention Project)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06805318
Acronym
RialSM
Enrollment
30
Registered
2025-02-03
Start date
2025-01-15
Completion date
2025-10-31
Last updated
2025-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis, Vocational Rehabilitation

Keywords

Multiple Sclerosis, Vocational Rehabilitation, Occupational Rehabilitation, Return to Work, Work Maintenance, Work Placement, Vocational Guidance, Reasonable Accomodation

Brief summary

Multiple sclerosis (MS) is an autoimmune demyelinating disease of the central nervous system with both inflammatory and degenerative characteristics that affects approximately 136,000 people in Italy. The highest incidence of disease onset occurs between the ages of 20 and 40, which corresponds to the most productive period of a person's life. For this reason, one of the main social consequences of MS is the reduction or abandonment of work activity, which often begins in the early stages of the disease. Vocational Rehabilitation (VR) interventions, as reported in the literature, are used to manage and reduce work-related difficulties. The goal of VR is to enable individuals who experience difficulties in performing work activities to access, find, and maintain employment. This approach is characterized by its multi-professional and multidimensional nature, involving different types of interventions carried out by various professionals in diverse settings. The overall aim of the project is to define a Vocational Rehabilitation (VR) protocol to reduce work-related challenges and promote job retention for workers with MS within the Italian healthcare and social context. The intervention will be organised into three different areas: rehabilitation, reasonable accommodation and education. Participants will receive any of the three interventions or a combination of these. The study will involve a multidisciplinary team of doctors (e.g. neurologist, physiatrist), psychologists, occupational therapists, physiotherapists, social workers, and labour law experts who will be involved according to the subject's specific needs.

Interventions

BEHAVIORALVocational Rehabilitation intervention for pwMS

The VR intervention will cover three areas of intervention: * Rehabilitation Area: this intervention has the goal of managing the work performance from a rehabilitative point of view. * Reasonable accommodation area: this intervention has the goal of assessing the needs of reasonable accommodations, such has workspace modification, change in organization of the activities, management of work time, etc.., and propose it to the employer. * Educational and Formative Area: this area is responsible for the implementation of educational intervention for the employees and the employers about multiple sclerosis and its impact on work performance, the rights and obligations of the employer and employee about disability management on the workplace.

Sponsors

Italian Multiple Sclerosis Society (AISM)Liguria, Genoa
CollaboratorUNKNOWN
IRCCS Santa Lucia Foundation, Rome
CollaboratorUNKNOWN
IRCCS San Martino Hospital, Genoa
CollaboratorUNKNOWN
Italian Workers' Compensation Authority (INAIL)
CollaboratorUNKNOWN
Department of Health Science (DiSSaL), University of Genoa, Genoa
CollaboratorUNKNOWN
Fondazione Italiana Sclerosi Multipla
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

The study design will be an explorative interventional pilot study. Participants will be recruited in the study among workers with MS in contact with AISM (Italian Multiple Sclerosis Society) Rehabilitation Service in Liguria, and Santa Lucia Foundation IRCCS, Rome. A sample of 30 workers with job difficulties (MSQ-Job\>=15) will be recruited for interventional study among subjects participating in a previous cross-sectional study. The VR intervention will be based on individual needs, covering three areas of intervention: the medical-rehabilitation area, the reasonable accommodation area, and the education area. During baseline evaluation, a maximum of 5 priority work difficulties will be identified for each subject. At the end of the VR intervention, the following aspects will be evaluated: resolution of work difficulties, satisfaction and effectiveness of the intervention through the Global Perceived Effect.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Confirmed MS diagnosis * Age ≥18 years * Currently employed at the beginning of the study entry * Have worked at least one day in the last 12 months * MSQ-Job \>=15 * Written informed consent

Exclusion criteria

* Presence of other pathologies impacting on work productivity

Design outcomes

Primary

MeasureTime frameDescription
InterceptionUp to 6 monthsNumber of eligible participants who has been invited to the VR intervention.
AcceptanceUp to 6 monthsNumber of participants who accepts to be included in the VR intervention.
AdherenceUp to 6 monthsNumber of participants who complete the VR intervention.
Lost to Follow-UpUp to 6 monthsNumber of dropouts from the VR intervention.
Canadian Occupational Performance Measure (COPM)Baseline, up to 6 monthsThe COPM employs a semi-structured interview that guides patients to define their concerns in three main areas: Self-care, Productivity - Paid or unpaid work, and Leisure. For the purposes of the study, only the Paid or unpaid work dimension will be assessed. Participants report two different scores regarding work activities' satisfaction and performance ranging from 1 to 10.
Client Satisfaction Questionnaire (CSQ)Up to 6 monthsThe Client Satisfaction Questionnaire collects data regarding satisfaction of participants on the VR intervention, using a 4 degree Likert scale ranging from one (not satisfied at all) to 4 (completly satisfied)
Global Perceived Effect (GPE) scaleUp to 6 monthsThis is a patient reported rating scale commonly used in clinical and research settings. For the purposes of the study, it is used to assess the overall perception of effectiveness related to the global VR Intervention in terms of reduction of work difficulties. A scale likert ranging from 1 to 7, where 1 indicates the lowest perceived effectiveness of the intervention on work difficulties, and 7 the highest perceived effectiveness.
Barthel Index (BI)Baseline, up to 6 monthsThe scale measures the level of autonomy in the basic activity of daily living. It assesses ten different basic activities of daily living: using the toilet, bathing, bowel functions, dressing, eating, walking, climbing stairs and moving from bed to chair. By assessing each of these functions it is possible to calculate an autonomy index ranging from 0 (totally dependent) to 100 (totally independent)
Hospital Anxiety Depression scale (HADS)Baseline, up to 6 monthsThe scale assesses the presence of mood disorders. It is one of the most self-reported questionnaires widely used in the hospital and research context. Its aim is to screen for the presence of anxiety and depression. It consists of 14 items used to define two separate scores for anxiety and depression. For both scores there is a cut-off (8) useful for classifying the clinical condition of the patient as healthy or pathological.
Modified Fatigue (MFIS-21)Baseline, up to 6 monthsThe scale measures fatigue level. It consists of 21 items, which can be summed up to define 3 dimensions of fatigue: physical, cognitive and social. Subjects can respond to the items with a likert scale ranging from 0 (no fatigue) to 4 (highest level of fatigue)
Multiple Sclerosis Neuropsychological Questionnaire for patient (MSNQ-p)Baseline, up to 6 monthsThe questionnaire identifies possible participants at risk for cognitive impairment. This is a 15 self-reported outcome aimed to assess the presence of cognitive impairment in pwMS. Items covered different domain of cognitive functioning: processing speed, dual-task processing, attention, memory, executive function, and psychosocial comportment. The response scale ranges from 0 to 4, where 0 is problem not encountered and 4 occurs very Frequently. A total maximum score of 60 is computed.
WHO Disability Assessment Schedule (WHODAS)Baseline, up to 6 monthsThe scale measures the impact of health conditions in daily life activities according to the Functioning, Disability and Health (ICF) framework. This questionnaire developed by the World Health Organization aimed to assess the impact of health status on client's level of functioning in six functional domains: cognition, mobility, self-care, getting along, life activities, participation. A score on a liker scale ranging from 1 to 5 indicates the impact of disability, with 1 indicating absence of impact and 5 the greatest possible impact. Each domain consists of five items. The score of each item are summed up to obtain a score for the individual functional domain. A total score is gained summing the total score of each functional domain.

Countries

Italy

Contacts

Primary ContactMichela Ponzio, PhD
michela.ponzio@aism.it+39 0102713246
Backup ContactMarco Salivetto, MS
marco.salivetto@aism.it+39 0102713832

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026