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Not yet recruitingNCT07211516Updated Oct 8, 2025

Relationship Between Cognition, Workforce Participation and Well-Being in Individuals With Multiple Sclerosis

An observational study in Multiple Sclerosis, sponsored by Region Gävleborg. Not yet recruiting at 1 site in Sweden. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2025-10-08.

Sponsored by Region Gävleborg · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
75
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
12th of 16
75 · median 179
Started
2026
with 3 others
Observational
16 of 91
5 open now
Primary completion
2026-11
later than 6 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 12th largest by planned enrollment of the 16 observational ones, is one of 4 that started in 2026, is one of 16 observational ones, reaches primary completion later than 6 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. 4 started in 2026.

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 examine factors important for work ability and well-being in persons with MS and cognitive impairments. The specific research questions are:

  1. How do job type and opportunities for workplace adaptations influence work ability and well-being in individuals with MS and cognitive impairments?
  2. What are the associations between cognitive function in MS and work ability as well as well-being? The investigators plan to collect data on patients with MS who have undergone a neuropsychological assessment at the neurology clinic in Region Gävleborg over a five year period. Approximately 100 patients are eligible for participation. Data will be collected through surveys and by extracting information from medical records. The surveys include questions related to well-being and work ability. Data from medical records contain data from the neuropsychological assessment, other rehabilitation interventions as well as data related to treatment and progress of MS.

The findings from the study 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 have performed a neuropsychological assessment during the 5 years prior to study start 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 Performed a neuropsychological assessment at the Neurology department at Gävle Hospital during the last 5 years (counting from study start) -

Exclusion criteria

Exclusion Criteria:

Other diagnosis hindering work participation more than MS

-

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
75 participants (estimated)
Patient registry
No

Groups and cohorts

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

    Time of neuropsychological assessment from 5 years before until study start.

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: Baseline

  2. Hospital anxiety and depression scale (HADS)

    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: Baseline

  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: Baseline

  4. Brief index of job satisfaction (BIAJS)

    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: Baseline

Secondary outcomes

  1. Work-life balance

    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: Baseline

  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: Baseline

07

Study locations

1 site
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 reached

Start is estimated for Apr 2026; primary completion for Nov 2026, 7 months later.

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

Registered
Sep 22, 2025
First posted
Oct 8, 2025
StartEst.
Apr 2026
Primary completionEst.
Nov 2026
CompletionEst.
Nov 2026
Last update
Oct 8, 2025
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 Oct 8, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07211516
Lead sponsor
Region Gävleborg
Collaborators
University of Gavle
Responsible party
Sponsor
First posted
Oct 8, 2025
Start date
Apr 2026 (estimated)
Primary completion
Nov 2026 (estimated)
Completion
Nov 2026 (estimated)
Last update
Oct 8, 2025

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 ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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Discussion

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