Complex regional pain syndrome Signs and Symptoms
Conditions
Interventions
The study methodology is an electronic-Delphi study, supported by face-to-face workshops. The stages are as follows:
1. Workshop 1: to consider expert opinion and the results of a syst
to consider those outcomes rated consistently most highly in the electronic Delphi Round 2 and to agree the draft ‘core clinical outcome measurement set’.
5. Experts in the field of CR
Sponsors
Royal United Hospitals Bath NHS Foundation Trust
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Participants must be a clinician, academic, industry representative or patient representative with expertise/experience in Complex Regional Pain Syndrome 2. Participants may be members of the International Association for the Study of Pain Special Interest Group for Complex Regional Pain Syndrome, members of the Complex Regional Pain Syndrome International Research Consortium, or members of the COMPACT consortium.
Exclusion criteria
Exclusion criteria: Not a clinician/academic/researcher working in the field of Complex Regional Pain Syndrome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of a core clinical outcome measurement set, agreed via collecting ratings of the relevance of clinical outcomes to the question "What is the clinical presentation and course of CRPS, and what factors influence it?". This method uses a Likert 1-9 rating scale at two timepoints: baseline and following feedback of baseline median group ratings | — |
Secondary
| Measure | Time frame |
|---|---|
| Modification of the existing COMPACT data management system is agreed by expert opinion, so that it can collect and store core outcome data from future clinical studies | — |
Countries
England, United Kingdom
Outcome results
None listed