Interdisciplinary treatment (IDT) + Clinical Decision Support System (CDSS)Interdisciplinary treatment (IDT)
Interdisciplinary treatment (IDT) + Clinical Decision Support System (CDSS): Interdisciplinary treatment (IDT) combined with Clinical Decision Support System (CDSS)
This cluster randomized controlled trial evaluates whether a person-centred, AI-supported Clinical Decision Support System (CDSS) can improve outcomes and cost-effectiveness in interdisciplinary rehabilitation for people with complex chronic pain. The CDSS is designed to assist clinicians in making personalized treatment decisions within standard interdisciplinary treatment (IDT). It has been developed using machine learning models trained on real-world data from over 100,000 patients in the Swedish Quality Registry for Pain Rehabilitation (SQRP), linked to several national registers, including the National Patient Register, the Prescribed Drug Register, the Social Insurance Agency database (MiDAS), and the Cause of Death Register. This enables individualized predictions of treatment outcomes, work ability, and healthcare utilization.
The trial includes 400 adult patients with chronic pain, enrolled at 20 IDT clinics randomized to either CDSS-supported or standard IDT. The study has three phases: feasibility, effectiveness, and implementation. The primary outcome is a patient-prioritized composite single-index of health-related well-being, based on domains such as pain, sleep, physical and mental health, emotional distress, and work ability. Patients prioritize these domains together with their clinical team, enabling a person-centred assessment. Secondary outcomes include HRQoL (EQ-5D, SF-36), emotional distress (HADS), and work ability (WAI), measured at baseline, post-treatment, 6- and 12-month follow-up.
A parallel mixed-methods process evaluation will examine implementation outcomes such as usability, clinician adherence, and workflow integration, using logs, surveys (e.g., S-NoMAD), and interviews. Normalization Process Theory guides the analysis. Cost-utility will be assessed using QALYs and ICERs from a societal perspective, with long-term projections using simulation models. Results will be reported in peer-reviewed publications.
Eligibility
Sex
ALL
Min age
18 Years
Max age
67 Years
Healthy volunteers
No
Inclusion Criteria:
* Aged 18 to 67 years
* Diagnosed with chronic non-malignant pain persisting longer than 3 months
* Pain condition includes, but is not limited to: fibromyalgia, widespread pain, back pain, neck pain, or shoulder pain
* Eligible for and referred to interdisciplinary rehabilitation (IDT) at a participating clinic
* Willing and able to participate in digital assessment and follow-up procedures
* Able to communicate and complete study materials in Swedish
* Provides written informed consent
Exclusion Criteria
* Pain caused by malignancy or cancer-related treatment
* Pain caused by systemic diseases such as rheumatoid arthritis, lupus, or other autoimmune or inflammatory conditions
* Severe psychiatric conditions interfering with study participation (e.g., untreated psychosis or severe depression requiring immediate psychiatric care)
* Documented cognitive impairment limiting ability to understand study participation or complete self-reported measures
* Currently enrolled in another interventional clinical trial that may confound the outcomes of this study
* Not expected to remain in the clinic's follow-up system for the duration of the study
Primary outcome measure(s)
Change from Baseline in Patient-Prioritized Health-Related Well-being Composite at 12 Months — (1) Baseline, (2) up to 18 weeks after baseline*, and (3) 12-month follow-up. (*Most programs last 6-8 weeks, but some clinics extend to 18 weeks (fewer sessions/week) due to existing routine practice). A person-centred composite score based on eight validated domains: pain intensity (NRS; 0-10), sleep problems (ISI; 0-28), physical health (SF-36 PF; 0-100), mental health (SF-36 MH; 0-100), depression and anxiety (HADS-A/D; 0-21), work ability (WAI single item; 0-10), and pain interference (single item; 0-10). At baseline, participants prioritize these domains together with the interdisciplinary treatment (IDT) team. The Clinical Decision Support System (CDSS) stores these weights. Each domain is normalized to 0-100 and combined into a weighted composite. Higher scores indicate better health-related well-being. Although composed of several scales, the outcome is reported as a single, aggregated primary measure.
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.
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