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RecruitingNCT07380295Updated Feb 2, 2026

Improving Workforce Participation and Well-Being in Individuals With Multiple Sclerosis - A Feasability Study

An observational study in Multiple Sclerosis, sponsored by Region Gävleborg. Recruiting at 1 site in Sweden. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-02-02.

Sponsored by Region Gävleborg · Observational

From the registry’s dates

  • Started Jul 2025; still recruiting 1 year 3 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
20
Ages
18 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 91 studies in Multiple Sclerosis with a site in Sweden — 10 open to participants now, 19 under way, 6 of them phase 3. Multiple Sclerosis · Sweden.

Planned enrollment
15th of 16
20 · median 179
Started
2025
with 4 others
Observational
16 of 91
5 open now
Primary completion
2028-09
later than 15 of 18 live
Registered
85th of 91
by date

Among the 91 studies in Multiple Sclerosis with a site in Sweden, this one is the 15th largest by planned enrollment of the 16 observational ones, is one of 5 that started in 2025, is one of 16 observational ones, reaches primary completion later than 15 of the 18 other live ones, and was the 85th registered.

By phase

91 studies; the count open now beside each. This study's row is marked.

Phase 336 · 1 open
Observationalthis study16 · 5 open
No phase14 · 4 open
Phase 212 · 0 open
Phase 410 · 0 open
Phase 12 · 0 open
Phase 1/21 · 0 open

By the year they started

First in 2002; this study’s year is marked. 5 started in 2025.

Size and results

Median enrollment 278 across the 75 interventional studies, 179 across the 16 observational. Of the 70 that completed or were terminated, 41 (59%) have results posted.

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Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 91 studies in Multiple Sclerosis with a site in Sweden, or all of them as a file.
02

Study summary

Multiple sclerosis (MS) is a chronic neurodegenerative disease and a leading cause of reduced workforce participation due to neurological illness in Western countries. Over the past 30 years, new treatments have reduced symptom burden, allowing patients to stay in the workforce longer. However, fatigue and cognitive impairments remain major barriers to work capacity. This project aims to preliminary examine the impact of cognitive function on work ability, and assess the role of neuropsychologists in multidisciplinary rehabilitation teams. It consists of a feasibility study evaluating the integration of neuropsychological interventions into teambased work-oriented rehabilitation. The specific research questions are:

  1. How can neuropsychological interventions be integrated into team-based work-oriented rehabilitation?
  2. How do these interventions relate to work ability and well-being in individuals with MS? The investigators plan to collect data on 20 consecutively patients with MS before, 6 months after and 2 years after a neuropsychological testing and intervention. The patients are being followed on measures related to well-being and work ability. Data from the neuropsychological assessment, other rehabilitation interventions as well as data related to treatment and progress of MS are also collected.

Our findings aim to enhance work-oriented rehabilitation and provide a deeper understanding of how to support individuals with MS in maintaining employment and overall well-being

03

Conditions studied

  • Multiple Sclerosis

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04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients of working age with MS in Region Gävleborg who are refered for a neuropsychological assessment and who are not suffering from other diagnosis which impact their work ability to a large extent.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Multiple sclerosis Age between 18-65 Refered to neuropsychological assessment at the Neurology departement at Gävle Hospital -

Exclusion criteria

Exclusion Criteria:

Other diagnosis hindering work participation more than MS

-

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
20 participants (estimated)
Target follow-up
2 Years
Patient registry
Yes

Groups and cohorts

  • Patients with multiple scleroris of working age

    Patients with MS and of working age (18-65) referred to neuropsychological evaluation.

06

What researchers measure

Primary outcomes

  1. Work participation

    Percentage of full-time work. 100 % full-time work and 0% is not working at all.

    Time frame: From baseline to 2-year follow-up

  2. Hospital anxiety and depression scale

    Self-assessment of anxiety and depression. Consists of two scales measuring the probability of having anxiety and depression respectively. Min score 0, max 21 for each scale. Higher scores indicate higher probability of anxiety/depression.

    Time frame: From baseline to 2-year follow-up

  3. WHO-5 Well-Being Index

    Overall rating of well-being. The WHO-5 score range is a raw score of 0-25, which is then multiplied by 4 to get a percentage score of 0-100. Higher score indicates higher well-being.

    Time frame: From baseline to 2-year follow-up

  4. Brief index of job satisfaction

    The Brief Index of Affective Job Satisfaction (BIAJS) has a score range of 1 to 5 for each of its four items, based on a 5-point Likert scale where 1 is "strongly disagree" and 5 is "strongly agree". The total BIAJS score is the sum of these four items, resulting in a possible range from 4 to 20, with higher scores indicating greater affective job satisfaction.

    Time frame: From baseline to 2-year follow-up

Secondary outcomes

  1. Quantative work demands

    Questions from the subscale "Quantitative demands" of the Copenhagen Psychosocial Questionnaire (COPSOQ-III) related to the demands of work. The COPSOQ-III uses Likert-like scales, and its items are coded with values of 0, 25, 50, 75, and 100 to achieve a 0-100 scale. Higher scores indicate more demands.

    Time frame: From baseline to 2-year follow-up

  2. Can-Work-S

    Three questions from a questionnaire developed to measure work-life balance after cancer. Each item ranges from 1 to 5 with higher scores indicating worse work-life balance.

    Time frame: From baseline to 2-year follow-up

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — To comply with the conditions set by the ethical review board, individual participant data (IPD) cannot be shared with other researchers. However, aggregated data are available upon reasonable reques

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2025 (actual). Primary completion is estimated for Sep 2028, 38 months after the start.

Of 334 non-industry observational studies under Multiple Sclerosis, half reached primary completion within 36 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 73. This study's planned 38 months is close to that.

Counting every sponsor, half of 425 studies reached it within 41 months; a quarter within 15 and three quarters within 75.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 22, 2025
First posted
Feb 2, 2026
StartActual
Jul 22, 2025
Primary completionEst.
Sep 2028
CompletionEst.
Sep 2028
Last update
Feb 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07380295
Lead sponsor
Region Gävleborg
Collaborators
University of Gavle
Responsible party
Sponsor
First posted
Feb 2, 2026
Start date
Jul 22, 2025
Primary completion
Sep 2028 (estimated)
Completion
Sep 2028 (estimated)
Last update
Feb 2, 2026

Study contacts

Natascha Ekdahl
Contact
natascha.ekdahl@regiongavleborg.se
+4626278023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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