No acute effects of placebo or open-label placebo treatments on strength, voluntary activation, and neuromuscular fatigue

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Bibliographische Detailangaben
Deutscher übersetzter Titel:Keine akuten Auswirkungen von Placebo- oder Open-Label-Placebo-Behandlungen auf Kraft, freiwillige Aktivierung und neuromuskuläre Ermüdung
Autor:Swafford, Alina P.; Kwon, Dennis P.; MacLennan, Rob J.; Fukuda, David H.; Stout, Jeffrey R.; Stock, Matt S.
Erschienen in:European journal of applied physiology
Veröffentlicht:119 (2019), 10, S. 2327–2338, Lit.
Format: Literatur (SPOLIT)
Publikationstyp: Zeitschriftenartikel
Medienart: Elektronische Ressource (online) Gedruckte Ressource
Sprache:Englisch
ISSN:1439-6319, 0301-5548
DOI:10.1007/s00421-019-04219-1
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Erfassungsnummer:PU202005003968
Quelle:BISp

Abstract des Autors

Purpose: Recent evidence suggests that deception may not be necessary for placebos to improve clinical outcomes. We tested the hypothesis that placebo and open-label placebo (OLP) treatments would acutely improve strength and voluntary activation, as well as minimize neuromuscular fatigue, in untrained participants.
Methods: Twenty-one males (n = 11) and females (n = 10) visited the laboratory on three occasions (placebo, OLP, control) to receive each treatment in a randomized, counter-balanced manner. Trials involved a pretest, a 15-min intervention, and posttests. For the placebo trial, participants were informed that they would be ingesting a capsule that would improve their performance and make them feel more energetic. For the OLP intervention, participants were told that the capsules would have no effects. In “Experiment #1”, knee extensor maximal voluntary contraction (MVC) peak torque and percent voluntary activation were evaluated. In “Experiment #2”, participants performed 20 consecutive MVCs while surface electromyographic signals were detected from the vastus lateralis. Subjective assessments of energy and perceived exertion were examined.
Results: The interventions had no effect on strength or voluntary activation, but energy levels increased following treatments (p = 0.016, η2 = 0.257). Neither treatment influenced neuromuscular fatigue. Though some variables showed moderate-to-large effect sizes, these results were consistent for individuals with lower voluntary activation.
Conclusion: Placebo and OLP treatments had minimal influence on strength, voluntary activation, and fatigue resistance. As these findings differ from recent reports, we speculate that placebos and OLPs are more likely to enhance muscle function in patient populations seeking medical care.