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Table 1 Schedule of enrolment, interventions, and assessments for the participants with CRPS

From: Pain reduction by inducing sensory-motor adaptation in Complex Regional Pain Syndrome (CRPS PRISMA): protocol for a double-blind randomized controlled trial

  1. RS Research Session, LTFU Long Term Follow-Up (postal questionnaires only), PA Prism Adaptations
  2. *Primary endpoint of the study
  3. **Secondary endpoint of the study
  4. ***Self-reported average levels of pain, range of movement and symptoms interference with daily life in the last 24 h, rated daily on 0–10 Numeric Rating Scales