Abstract
Background. Conditioned pain modulation (CPM) is measured by comparing pain induced by a test stimulus with pain induced by the same test stimulus, either during (parallel design) or after (sequential design) the conditioning stimulus. Whether design, conditioning stimulus intensity and test stimulus selection affect CPM remains unclear. Methods. CPM effects were evaluated in healthy participants (N D 89) at the neck, forearm and lower leg using the cold pressor test as the conditioning stimulus. In three separate experiments, we compared the impact of (1) design (sequential versus parallel), (2) conditioning stimulus intensity (VAS 40/100 versus VAS 60/100), and (3) test stimulus selection (single versus dual, i.e., mechanical and thermal). Statistical analyses of the main effect of design (adjusted for order) and experiment were conducted using linear mixed models with random intercepts. Results. No significant differences were identified in absolute CPM data. In relative CPM data, a sequential design resulted in a slightly lower CPM effect compared to a parallel design, and only with a mechanical test stimulus at the neck (-6.1%; 95% CI [-10.1 to -2.1]) and lower leg (-5.9%; 95% CI [-11.7 to -0.1]) but not forearm (-4.5%; 95% CI [-9.0 to 0.1]). Conditioning stimulus intensity and test stimulus selection did not influence the CPM effect nor the difference in CPM effects derived from parallel versus sequential designs. Conclusions. Differences in CPM effects between protocols were minimal or absent. A parallel design may lead to a minimally higher relative CPM effect when using a mechanical test stimulus. The conditioning stimulus intensities assessed in this study and performing two test stimuli did not substantially influence the differences between designs nor the magnitude of the CPM effect.
Original language | English |
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Article number | e12330 |
Pages (from-to) | 1-27 |
Number of pages | 27 |
Journal | PeerJ |
Volume | 9 |
DOIs | |
Publication status | Published - 14 Dec 2021 |
Bibliographical note
Funding Information:This study was conducted with a research grant for teachers of the Dutch Organisation of Scientific Research (NWO) under project number 023.011.069. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
The following grant information was disclosed by the authors: The Dutch Organisation of Scientific Research (NWO) under project number 023.011.069.
Publisher Copyright:
© 2021 PeerJ Inc.. All rights reserved.
Funding
This study was conducted with a research grant for teachers of the Dutch Organisation of Scientific Research (NWO) under project number 023.011.069. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The following grant information was disclosed by the authors: The Dutch Organisation of Scientific Research (NWO) under project number 023.011.069.
Funders | Funder number |
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Dutch Organisation of Scientific Research | |
Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 023.011.069 |
Keywords
- Pain modulation
- Endogenous pain inhibition
- Pain measurement
- Pain assessment
- Central pain mechanisms
- Central sensitisation
- Nociceptive pain
- Experimental pain
- Pain threshold
- Central pain processing