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Research on agreement and experiences with the nociplastic pain criteria

The reliability and clinical experience of the IASP clinical criteria and grading system for nociplastic pain - The reliability and clinical experience of the IASP clinical criteria and grading system for nociplastic pain

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON61444
Enrollment
40
Registered
2026-07-23
Start date
2026-10-01
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Nociplastic pain Pain due to altered signal processing

Interventions

IASP clinical criteria and grading system for nociplastic pain.&nbsp

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Practicing and registered as physiotherapist, pain specialist, rehabilitation physician or general practitioner.  At least three years of experience in chronic pain discrimination (in primary, secondary or tertiary setting).  Sufficient proficiency in the Dutch language to understand study information, provide informed consent, or complete study procedures/questionnaires. 

Exclusion criteria

Exclusion criteria: Less than three years of experience in chronic pain discrimination (in primary, secondary or tertiary setting). Insufficient proficiency in the Dutch language to understand study information, provide informed consent, or complete study procedures/questionnaires. 

Design outcomes

Primary

MeasureTime frame
For the primary research question we will determine: Absolute agreement for the dichotomous (all subquestions) and ordinal (final classification of the vignettes) outcome intra-observer reliability dichotomous (all subquestions) and ordinal (classification of the vignettes) outcome Inter-observer reliability dichotomous (all subquestions) and ordinal (classification of the vignettes) outcome 

Secondary

MeasureTime frame
For the secondary research question we will determine themes describing the clinical experiences with the criteria and grading system per discipline.  

Countries

Netherlands

Contacts

Public ContactJ.C. Schouten

Erasmus MC, Universitair Medisch Centrum Rotterdam

J.c.schouten@erasmusmc.nl0650162221

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 25, 2026