- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06805318
Feasibility of a Vocational Rehabilitation Intervention for Job Retention in Workers With MS-RiaLSM Intervention Project (RialSM)
Development and Assessment of a Vocational Rehabilitation Intervention for Job Retention in Workers With Multiple Sclerosis (RiaLSM Intervention Project)
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Michela Ponzio, PhD
- Phone Number: +39 0102713246
- Email: michela.ponzio@aism.it
Study Contact Backup
- Name: Marco Salivetto, MS
- Phone Number: +39 0102713832
- Email: marco.salivetto@aism.it
Study Locations
-
-
Lazio
-
Rome, Lazio, Italy, 00179
- Not yet recruiting
- Irccs Fondazione Santa Lucia
-
Contact:
- Maria Grazia Grasso, PhD
- Phone Number: +39 0651501920
- Email: mg.grasso@hsantalucia.it
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-
Liguria
-
Genoa, Liguria, Italy, 16149
- Recruiting
- Servizio di Riabilitazione AISM Liguria, Italian Multiple Sclerosis Society
-
Contact:
- Giampaolo Brichetto, PhD
- Phone Number: +39 0102713532
- Email: giampaolo.brichetto@aism.it
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: VR intervention
This is a single-arm study.
Therefore, the intervention will be conducted on the whole sample.
The nature of the rehabilitation program will vary and will cover three different areas: the rehabilitation area, the reasonable accommodation area, and the educational and formative area.
Participants can receive any of the three types of intervention, or a combination of these, based on individual needs.
|
The VR intervention will cover three areas of intervention:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Interception
Time Frame: Up to 6 months
|
Number of eligible participants who has been invited to the VR intervention.
|
Up to 6 months
|
|
Acceptance
Time Frame: Up to 6 months
|
Number of participants who accepts to be included in the VR intervention.
|
Up to 6 months
|
|
Adherence
Time Frame: Up to 6 months
|
Number of participants who complete the VR intervention.
|
Up to 6 months
|
|
Lost to Follow-Up
Time Frame: Up to 6 months
|
Number of dropouts from the VR intervention.
|
Up to 6 months
|
|
Canadian Occupational Performance Measure (COPM)
Time Frame: Baseline, up to 6 months
|
The 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.
|
Baseline, up to 6 months
|
|
Client Satisfaction Questionnaire (CSQ)
Time Frame: Up to 6 months
|
The 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)
|
Up to 6 months
|
|
Global Perceived Effect (GPE) scale
Time Frame: Up to 6 months
|
This 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.
|
Up to 6 months
|
|
Barthel Index (BI)
Time Frame: Baseline, up to 6 months
|
The 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)
|
Baseline, up to 6 months
|
|
Hospital Anxiety Depression scale (HADS)
Time Frame: Baseline, up to 6 months
|
The 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.
|
Baseline, up to 6 months
|
|
Modified Fatigue (MFIS-21)
Time Frame: Baseline, up to 6 months
|
The 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)
|
Baseline, up to 6 months
|
|
Multiple Sclerosis Neuropsychological Questionnaire for patient (MSNQ-p)
Time Frame: Baseline, up to 6 months
|
The 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.
|
Baseline, up to 6 months
|
|
WHO Disability Assessment Schedule (WHODAS)
Time Frame: Baseline, up to 6 months
|
The 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.
|
Baseline, up to 6 months
|
Collaborators and Investigators
Collaborators
Investigators
- Study Director: Giampaolo Brichetto, PhD, Fondazione Italiana Sclerosi Multipla
Publications and helpful links
General Publications
- Vitturi BK, Rahmani A, Dini G, Montecucco A, Debarbieri N, Bandiera P, Ponzio M, Battaglia MA, Brichetto G, Inglese M, Persechino B, Durando P. Work Barriers and Job Adjustments of People with Multiple Sclerosis: A Systematic Review. J Occup Rehabil. 2023 Sep;33(3):450-462. doi: 10.1007/s10926-022-10084-1. Epub 2022 Nov 18.
- Ponzio M, Pignattelli E, Verri A, Grange E, Persechino B, Vitturi BK, Bandiera P, Manacorda T, Inglese M, Durando P, Battaglia MA. Job Retention by People With Disabilities: A Qualitative Study of the Perspectives of People With Multiple Sclerosis. Med Lav. 2024 Jun 21;115(3):e2024018. doi: 10.23749/mdl.v115i3.15947.
- Ponzio M, Podda J, Pignattelli E, Verri A, Persechino B, Vitturi BK, Bandiera P, Manacorda T, Inglese M, Durando P, Battaglia MA. Work Difficulties in People with Multiple Sclerosis. J Occup Rehabil. 2024 Sep;34(3):606-617. doi: 10.1007/s10926-023-10149-9. Epub 2023 Nov 3.
- Sweetland J, Riazi A, Cano SJ, Playford ED. Vocational rehabilitation services for people with multiple sclerosis: what patients want from clinicians and employers. Mult Scler. 2007 Nov;13(9):1183-9. doi: 10.1177/1352458507078414. Epub 2007 Jul 10.
- Escorpizo R, Reneman MF, Ekholm J, Fritz J, Krupa T, Marnetoft SU, Maroun CE, Guzman JR, Suzuki Y, Stucki G, Chan CC. A conceptual definition of vocational rehabilitation based on the ICF: building a shared global model. J Occup Rehabil. 2011 Jun;21(2):126-33. doi: 10.1007/s10926-011-9292-6.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CET Liguria:329/2024-DBid13998
- Grant BRic 2022, ID 31 (Other Grant/Funding Number: Supported by INAIL - Italian Workers' Compensation Authority)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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