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Clinical Trials in Norway / NCT06110468
Active, not recruiting Not applicable

Physical Function, Health and Employment for People With Multiple Sclerosis

NCT06110468 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2024-03-04
Last updated
2024-11-21

Condition(s) studied

Multiple Sclerosis

Investigational drug(s) / intervention(s)

CoreDISTParticipation

CoreDISTParticipation: CoreDISTparticipation is a multi-disciplinary individualized intervention that concurrently combine 1) providing PwMS and their employers with information on MS, possibilities for work-adaptations within the welfare system and the importance of physical activity 2) Structured goal-setting regarding reducing barriers for work and regarding physical function and activity for PwMS 3) A physiotherapy intervention focusing on improving the underlying prerequisites for balance and walking along with high intensive training and promotion of physical activity 4) structured evaluation and adjustment of goals.

Study summary

Employment is low in people with MS, even when physical levels of functioning are high. The purpose of this study is to investigate if an individually tailored intervention combining individualized physiotherapy and work adaptation works better than usual care in terms of reducing barriers for work and improving levels of physical activity. The utility of the intervention will be investigated in terms of quality adjusted life years, long-term employment status and work-related costs.

Eligibility

Sex
ALL
Min age
18 Years
Max age
67 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosed with Multiple Sclerosis according to the McDonald's criteria * Extended Disability Status Scale (EDSS) 0-4 * Being employed, part time or full time, may include various degrees of sick leave, disability pension or AAP. * Living in the participating 18 municipalities (Hammerfest, Alta, Senja, Målselv, Tromsø, Harstad, Narvik, Fauske, Bodø, Meløy, Vågan, Vestvågøy, Sortland, Hadsel, Rana, Vefsn, Alstadhaug, Brønnøy). Exclusion Criteria: * Pregnancy at enrolment. * Exacerbation of symptoms (i.e. relapse) within two weeks prior to enrolment. * Other serious conditions.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Nordlandssykehuset HF Bodø Nordland

More Nordlandssykehuset HF trials in Norway

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06110468 on ClinicalTrials.gov ↗ ← All trials in Norway