Actively Recruiting

Age: 18Years +
All Genders
ID07603674

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Malignant and inflammatory diseases
  • Unable to understand spoken and written Swedish

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for eligibility assessment

Monitoring

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

Surveillance

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

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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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