Systematic ReviewPain Science & Central SensitizationDiagnosis & AssessmentSystematic Reviews & Meta-analysesClinical RelevanceDOI
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Among eight questionnaires for measuring central sensitization in chronic pain, the Central Sensitization Inventory (CSI) currently has the strongest and most reliable evidence, though none of the tools has been fully validated yet.

Bottom line

The CSI appears to be the most reliable patient-reported tool for assessing central sensitization in chronic pain, but evidence for all instruments remains incomplete and more validation research is needed.

Moderate evidence

Published

2025
1 years ago
Current

Evidence hierarchy

Meta-analysis
Systematic Review ◀ this study
RCT
Cohort
Case-Control
Case Report
Expert Opinion

Study participants

58 studies; per-study participant counts ranged from 31 to 1651Mean patient age 48 years (SD 11.8)Predominantly female; several studies enrolled only female participants and the rest had more women than men

Adults with chronic pain conditions including fibromyalgia, chronic low back pain, neck pain, chronic widespread pain, and mixed/musculoskeletal pain

Full research — for clinicians and curious readers

Study Summary

This systematic review and meta-analysis, conducted using COSMIN guidelines, identified and appraised the measurement quality of eight patient-reported outcome measures (PROMs) used to assess central sensitization (CS) in adults with chronic pain. Across 58 included studies, most instruments had limited evidence for their psychometric properties, often reflecting few publications and doubtful or inadequate study methodology rather than necessarily poor instruments. The Central Sensitization Inventory (CSI) received the highest overall ratings (sufficient on six of nine measurement properties, with moderate-to-high quality of evidence), followed by the Pain Sensitivity Questionnaire (PSQ) and Fibromyalgia Survey Questionnaire (FSQ). Pooled test-retest reliability was excellent for the CSI (ICC 0.93 overall chronic pain) and PSQ (ICC 0.86), though heterogeneity was high and no PROM had been evaluated across all nine measurement properties.

76/100
Evidence StrengthStrong
Study Quality
Sample Size
Replication

Key Findings

The Central Sensitization Inventory (CSI) had the strongest measurement evidence of the eight instrumentsHigh

CSI was the most frequently studied PROM (37 studies) and was rated 'sufficient' for content validity, structural validity, internal consistency, reliability, construct validity (83% of results aligned with hypotheses), and responsiveness, with high-quality evidence for most properties.

Pooled test-retest reliability of the CSI was excellentHigh

Random-effects meta-analysis of 17 studies gave an ICC of 0.93 (95% CI 0.91-0.95) for overall chronic pain, 0.90 (95% CI 0.87-0.93) for chronic musculoskeletal pain, and 0.93 (95% CI 0.88-0.99) for chronic neck pain, though heterogeneity was substantial (I-squared 70.7-94.4%).

The Pain Sensitivity Questionnaire (PSQ) also showed excellent test-retest reliabilityMedium

Pooled ICC for PSQ was 0.86 (95% CI 0.72-0.99, I-squared 87.4%) in chronic pain, but it was rated 'insufficient' for construct validity because 25% of study results did not align with hypotheses.

Most PROMs had limited psychometric evidenceHigh

Five of the eight instruments (NFF, GPQ, SHS, a Novel Self-report Questionnaire, and L-VISS/VDS) had measurement properties assessed in only a single study each, and no instrument had been evaluated across all nine COSMIN measurement properties.

Study methodological quality was frequently doubtful or inadequateMedium

Common shortcomings included unclear reporting of the content-validation process, absence of factor analysis before computing internal consistency, failure to calculate the minimal important change (MIC) for measurement error, and unassessed cross-cultural validity despite 42 studies evaluating translated versions.

Study Methodology
Study Design
Systematic review and meta-analysis conducted per COSMIN guidelines and reported following PRISMA-COSMIN; protocol registered in PROSPERO (CRD42023460050). Six databases (MEDLINE, EMBASE, SCOPUS, PubMed, Web of Science, CINAHL) searched from inception to September 2023. Random-effects meta-analysis (REML) of test-retest reliability (ICC) for the CSI and PSQ.
Sample Size
58 studies; participant counts per study ranged from 31 to 1651
Duration
Databases searched from inception to September 2023
Population
Adults with chronic pain conditions (e.g., fibromyalgia, chronic low back pain, neck pain, chronic widespread pain, musculoskeletal pain, mixed chronic pain); mean patient age 48 years (SD 11.8); studies skewed toward female participants, with several female-only samples
Outcome Measures
COSMIN risk-of-bias checklist (methodological quality) · Updated COSMIN criteria for good measurement properties · Modified GRADE for level of evidence · Pooled intraclass correlation coefficient (ICC) for test-retest reliability · Heterogeneity (Q statistic, I-squared)

Strengths

  • Identified all available PROMs for central sensitization manifestations in chronic pain rather than a single instrument
  • Used the most current COSMIN methodology for systematic appraisal of both study quality and instrument psychometric properties
  • Pooled reliability quantitatively in a random-effects meta-analysis where data allowed
  • Dual independent reviewers with expert adjudication of conflicts
  • Protocol pre-registered (PROSPERO CRD42023460050) and reported per PRISMA-COSMIN

Limitations

  • The COSMIN-based rating system can be subject to reviewer subjectivity, despite consensus procedures
  • Only English-language studies were included, excluding three studies on the CSI and PSQ published in other languages (language bias)
  • Findings are based only on adult populations and may not generalize to pediatric patients
  • Substantial statistical heterogeneity in the pooled reliability estimates (I-squared up to 94.4%)
  • Most instruments had measurement properties assessed in very few (often single) studies, and many included studies had doubtful or inadequate methodological quality
  • Publication bias could not be formally assessed, as no accepted method exists for systematic reviews of PROM measurement properties

Key Takeaways for Patients

What This Means for You

  1. 01Central sensitization is a process where the nervous system becomes overly sensitive, so pain can persist even when there is no clear ongoing tissue damage.
  2. 02Questionnaires that ask about your own symptoms (patient-reported outcome measures) are a standard, accepted way to assess this kind of pain.
  3. 03Of the eight questionnaires reviewed, the Central Sensitization Inventory (CSI) had the strongest and most consistent evidence and produced very stable results when the same people retook it.
  4. 04No single questionnaire has been fully validated on every quality measure yet, so clinicians should choose the assessment tool carefully and more research is still needed.

Read the Full Paper

Access the complete peer-reviewed study from Journal of Patient-Reported Outcomes

View Full Study

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