Actively Recruiting
Precision-based Care for People With Musculoskeletal Conditions Seeking Primary Health Care: Enhancing Recovery and Health Outcomes
Led by Karolinska Institutet · Updated on 2026-05-22
300
Participants Needed
1
Research Sites
78 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the Start-MSK tool, a screening instrument designed to support personalized treatment for adults with musculoskeletal pain. This tool aims to identify risk levels for long-term pain and disability, helping to direct appropriate care. The study involves 300 patients aged 18 and older seeking primary care rehabilitation and physiotherapy in several Swedish regions. The goal is to investigate whether Start-MSK can predict treatment outcomes such as pain and quality of life at 3 and 6 months, and to explore patient and physiotherapist experiences with the tool in shared decision-making. Participants will receive usual physiotherapy care while the Start-MSK tool is used at the first visit to classify patients into low, medium, or high risk for persistent pain. Physiotherapists will use the tool’s results to guide treatment discussions but are not directed to alter treatment based on risk. Treatment details, including session numbers and types such as exercise or mobilization, will be collected through surveys at 8 weeks. There is no experimental treatment; the focus is on observing outcomes linked to the tool’s risk stratification. Patients will complete web-based questionnaires at baseline, 8 weeks, 3 months, and 6 months, reporting on pain, function, quality of life, and recovery. Physiotherapists will provide treatment data and participate in interviews or focus groups to share their views on the tool’s use. The study measures include the Start-MSK tool scores, musculoskeletal pain screening questionnaires, and quality of life assessments. Follow-up lasts 6 months, during which researchers monitor outcomes and experiences to assess the tool’s validity and usability in primary care.
CONDITIONS
Brief Title
Precision Based Primary Care for Patients With Musculoskeletal Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with musculoskeletal pain in neck, back, shoulder, hip, knee, or multiple sites
- Recruited from primary care
- Aged 18 years and older
You will not qualify if you...
- Malignant and inflammatory diseases
- Unable to understand spoken and written Swedish
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) for eligibility assessment
Duration - 6 months
Participants complete self-report questionnaires on musculoskeletal pain, quality of life, and psychosocial factors at baseline, 8 weeks, 3 months, and 6 months. Physiotherapists report treatments given at 8 weeks.
Questionnaires completed via web-based system at baseline, 8 weeks, 3 months, and 6 months; 1 treatment report at 8 weeks
Duration - Around 3 months
Participants and physiotherapists provide qualitative feedback through interviews or focus groups around 3 months to explore experiences with the stratification tool and shared decision-making.
1 to 2 interviews or focus group sessions depending on participant group
Trial Site Locations
Total: 1 location
1
Karolinska Institutet
Stockholm, Sweden
Actively Recruiting
Research Team
E
Eva Rasmussen Barr, Associate professor PhD
P
Philip von Rosen, Associate professor, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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