CSS-SR Validation Study
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Alexandra Sideris, PhD · PRINCIPAL_INVESTIGATOR · Hospital for Special Surgery, New York
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Concordance between CSS-Clinician and CSS-SR total scoresDate of enrollment
Concordance between CSS-Clinician total scores, which will be on a numerical scale potentially ranging from 0-16, and CSS-SR total scores, which will be on a numerical scale potentially ranging from 0-13. Higher scores indicate greater CRPS symptom severity while lower scores indicate a lesser degree of symptom severity. Concordance (corrected for chance agreement) between CSS-Clinician and CSS-SR items and total scores will be assessed using intraclass correlations (ICCs; two-way random effects model; potential range = -1.00 to 1.00). Strength of agreement will be evaluated for descriptive purposes based on published recommendations: \< 0.50 = poor agreement, 0.50 - 0.75 = moderate agreement, 0.76 - 0.90 = good agreement, and \>0.90 = excellent agreement. All analyses will use the maximum number of cases available with a two-sided p\<0.05 criterion for statistical significance.