Accurate pain reporting training diminishes the placebo response: Results from a randomised, double-blind, crossover trial
- PMID: 29795665
- PMCID: PMC5993117
- DOI: 10.1371/journal.pone.0197844
Accurate pain reporting training diminishes the placebo response: Results from a randomised, double-blind, crossover trial
Abstract
Analgesic trials frequently fail to demonstrate efficacy of drugs known to be efficacious. Poor pain reporting accuracy is a possible source for this low essay-sensitivity. We report the effects of Accurate-Pain-Reporting-Training (APRT) on the placebo response in a trial of Pregabalin for painful-diabetic-neuropathy. The study was a two-stage randomized, double-blind trial: In Stage-1 (Training) subjects were randomized to APRT or No-Training. The APRT participants received feedback on the accuracy of their pain reports in response to mechanical stimuli, measured by R-square score. In Stage-2 (Evaluation) all subjects entered a placebo-controlled, cross-over trial. Primary (24-h average pain intensity) and secondary (current, 24-h worst, and 24-h walking pain intensity) outcome measures were reported. Fifty-one participants completed the study. APRT patients (n = 28) demonstrated significant (p = 0.036) increases in R-square scores. The APRT group demonstrated significantly (p = 0.018) lower placebo response (0.29 ± 1.21 vs. 1.48 ± 2.21, mean difference ± SD = -1.19±1.73). No relationships were found between the R-square scores and changes in pain intensity in the treatment arm. In summary, our training successfully increased pain reporting accuracy and resulted in a diminished placebo response. Theoretical and practical implications are discussed.
Conflict of interest statement
SEH has received research funding from Cerephex, Eli Lily, Forest Laboratories, and Merck; and served as a consultant for Pfizer, Analgesic Solutions, Aptinyx, and deCode Genetics. He is also co-inventor of the MAST pain testing device and a member of Arbor Medical Innovations, LLC (Ann Arbor, MI). GHK is a co-inventor of the MAST and a member of Arbor Medical Innovations (AMI), LLC, which assisted in providing the MAST systems used as part of this study. He has also served as a consultant to Analgesic Solutions and deCode Genetics. NPK is the CEO of Analgesic Solutions, a clinical research and consulting firm with many clients throughout the pharmaceutical industry. RT and OL are employees of Analgesic Solutions. NK and JDS are former employees of Analgesic Solutions. JB and MF are employees of Grunenthal. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
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