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Study identifier: NCT06583980 Synced from ClinicalTrials.gov · July 29, 2026
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INSELMA - a Randomised Controlled Trial

Condition: Rheumatoid Arthritis · Psoriatic Arthritis · Axial Spondyloarthritis  ·  Sponsor: The Danish Center for Expertise in Rheumatology

PhaseNA
Planned participants120
Who can joinAll sexes, 18 Years to 100 Years
Healthy volunteersNo

About this study

Background: Patients with inflammatory arthritis (IA) experience substantial impact of their disease despite optimal pharmacological treatment. To be able to manage these challenges effectively, patients require tailored self-management support from various professionals. We thus developed a six-month nurse-coordinated interdisciplinary self-management intervention (INSELMA), in collaboration with patients, clinicians and managers. A pilot study on the INSELMA intervention in 18 participants showed promising results. It is now relevant to test the intervention and compare it to a control group in a larger study . Objectives: The primary objective is to compare the efficacy of the INSELMA intervention to usual care (control group), on health related quality of life measured at baseline and end of intervention (6 months after baseline). Key secondary objectives are to compare the short and longer-term effect of INSELMA on changes in mental well-being, anxiety, depression, fatigue, pain, sleep, physical activity, global impact of the disease, work ability, self-efficacy for managing chronic disease and pain and health literacy relative to usual care from baseline to 6 and 12 months after baseline and on quality of life from baseline to 12 months after baseline. Method: A pragmatic randomised trial with a two-group parallel design. All participants will be randomly allocated to the intervention or usual care only . Both groups will receive usual care. The INSELMA interven…

This description comes directly from the study's public registry record.

Talk to the study team

Jette Primdahl, PhD  ·  0045 2420 6692  ·  jprimdahl@danskgigthospital.dk

Bente Appel Esbensen, PhD  ·  0045 2441 2490  ·  bente.appel.esbensen@regionh.dk

Always discuss trial participation with your own doctor first.

Locations (3)

Frederiksberg HospitalFrederiksberg, DenmarkRecruiting
Rigshospitalet-GlostrupGlostrup Municipality, DenmarkRecruiting
Danish Hospital for Rheumatic DiseasesSønderborg, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT06583980