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Optimizing management of musculoskeletal pain disorders in primary physiotherapy care

An AI-based clinical decision support system for personalized care of common musculoskeletal pain disorders in primary physiotherapy care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17927832
Enrollment
720
Registered
2021-01-18
Start date
2021-02-01
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Improved treatment outcome for patients with common musculoskeletal disorders such as neck, shoulder, low back, hip, knee and multisite pain Musculoskeletal Diseases

Interventions

To implement personalized care, we will employ innovative methods from artificial intelligence (AI) in terms of Case-Based Reasoning (CBR) to build a clinical decision support system (cDSS) based on p

Sponsors

Norwegian University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 110 Years

Inclusion criteria

Inclusion criteria: 1. Patients presenting to a primary care physiotherapist with musculoskeletal pain disorder in any of these areas; shoulder, neck, upper/low back, hip, knee or with multisite pain as primary contact reason. 2. Age above 18 years 3. Physiotherapists with the patient participants in their current patient population

Exclusion criteria

Exclusion criteria: 1. Reduced cognitive function or skills in Norwegian (impeding reading, speaking or comprehension of Norwegian language) 2. Neurological diagnosis (e.g. multiple sclerosis, stroke, ALS, Parkinson, dementia) 3. On-going cancer 4. Pregnancy or pregnancy-related disorders 5. Scheduled for surgery or recent surgery or fracture within the last 6 months

Design outcomes

Primary

MeasureTime frame
1. Patients' assessment of their condition measured by Global perceived effect (GPE), a seven-point Likert scale, at 3, 6 and 12 months. The GPE scale will be dichotomized as “improved” (score 1-2) or "unchanged/worse" (score 3-7). 2. Clinically important improvement in function, measured by the Patient Specific Function Scale (PSFS; 0-10), where a 30% change is defined as a Minimal clinically important difference (MCID). PSFS will be measured at baseline, 2, 4, 8 and 12 weeks

Secondary

MeasureTime frame
At baseline and 3, 6 and 12 month follow-up secondary outcomes include: 1. Pain intensity (NRS; 0-10) 2. Pain drawing, number of pain sites 3. Pain mapping; how often, continuous (of and on), daily variation 4. EQ-5D-5L (quality of life), five items 5. 15D (health-related quality of life, two items; sleep and vitality 6. Musculoskeletal Health Questionnaire (MSK-HQ) 7. Number of treatments by 3 months (patient records) 8. Patient-specific functional scale (PSFS; 0-10) 9. Work ability (single item from Work Ability Index; current work ability compared with life-time best 10. Work status/sick leave (patient records) 11. Medication (patient records) 12. Patient-therapist relationship (3 questions); overall satisfaction, belief in therapist's competency, and communication 13. Benefits of physiotherapy and expectations to physiotherapist (2 questions) 14. Adherence to treatment plan (5 alternatives) 15. Goal achievement (not, partly, or fully achieved) (patient records) 16. Most important reason for success/non-success (text), at 3 months only 17. Still receiving physiotherapy after 3, 6 and 12 months (yes/no) 18. Physical activity, 3 questions; frequency, intensity and duration 19. Hopkins Symptom Check List, HSCL-10 (emotional distress) 20. Pain Self efficacy, 2 questions (from PSEQ 2-item) 21. Cost-utility based on patients deductibles and costs covered by the Norwegian Health Economics Administration (HELFO) and utility measured by EQ-5D At 2, 4 and 8 weeks secondary outcomes collected by SMS (text-messages): 1. Patient-specific functional scale 2. Work ability 3. Global perceived effect score 4. Pain intensity, at 2 and 8 weeks only 5. Pain self-efficacy, at 2 and 8 weeks only

Countries

Norway

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: May 7, 2026