Effects of Hypnotic Analgesia and Transcranial Direct Current Stimulation on Pain Tolerance and Corticospinal Excitability in Individuals with Fibromyalgia: A Cross-Over Randomized Clinical Trial

J Pain Res. 2023 Jan 24:16:187-203. doi: 10.2147/JPR.S384373. eCollection 2023.

Abstract

Objective: We compare the effect of HAS, a-tDCS on the left dorsolateral prefrontal cortex (l-DLPFC), and rest-testing on pain measures [(cold pressor test (CPT) (primary outcome) and heat pain threshold]. We also compare their effects on the motor evoked potential (MEP) (primary outcome), short intracortical inhibition (SICI), intracortical facilitation (ICF), and cortical silent period (CSP).

Methods: This randomized, blind, crossover trial included 18 women with fibromyalgia, aged from 18 to 65 years old. They received at random and in a crossover order a-tDCS over the l-DLPFC (2mA), HAS, or a rest-testing.

Results: HAS compared to a-tDCS increased the pain tolerance with a moderate effect size (ES) [Cohen's f=-0.78; (CI 95%; -1.48 to -0.12)]. While compared to rest-testing, HAS increased the CPT with a large ES [Cohen's f=-0.87; (CI 95%; -1.84 to -0.09)]. The a-tDCS compared to HAS increased the MEP amplitude with large ES [Cohen's f=-1.73 (CI 95%; -2.17 to -0.17)]. Likewise, its ES compared to rest-testing in the MEP size was large [Cohen's f=-1.03; (CI 95%; -2.06 to -0.08)].

Conclusion: These findings revealed that HAS affects contra-regulating mechanisms involved in perception and pain tolerance, while the a-tDCS increased the excitability of the corticospinal pathways. They give a subsidy to investigate their effect as approaches to counter regulate the maladaptive neuroplasticity involved in fibromyalgia.

Clinical trial registration: www.ClinicalTrials.gov, identifier - NCT05066568.

Keywords: CPM-test; chronic pain; cold pressor test; fibromyalgia; hypnosis; hypnotic analgesia; pain threshold; tDCS.

Publication types

  • Case Reports
  • Clinical Trial

Associated data

  • ClinicalTrials.gov/NCT05066568

Grants and funding

The present research was supported by the following Brazilian funding agencies: (i) Committee for the Development of Higher Education Personnel – CAPES PROEX (grant to BS with master scholarship, Grant #2020). (ii) National Council for Scientific and Technological Development – CNPq (grant to WC number: 420826/2018-1). (iii) Foundation for the Support of Research at Rio Grande do Sul (FAPERGS) Ministry of Science and Technology. National Council for Scientific and Technological Development – (CNPq)/ Health Secretary of state of Rio Grande do Sul, Brazil (SEARS) n. 03/2017 (PPSUS) (number: 17/2551-0001). (iv) Brazilian Innovation Agency (FINEP [Financiadora de Estudos e Projetos]) (process number 1245/13). (v) FINEP grant 0261/18 chamada pública MCTIC/FINEP/CT-INFRA 04/2018. (vi) Fundação de incentivo à Pesquisa (FIPE) at Hospital de Clínicas de Porto Alegre.