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首页> 外文期刊>Applied neuropsychology. Adult >The Effects of Cold Pressor-Induced Pain on PASAT Performance
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The Effects of Cold Pressor-Induced Pain on PASAT Performance

机译:冷压诱发的疼痛对PASAT性能的影响

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Although clinicians have frequently observed that patients with chronic pain experience cognitive deficits related to memory and concentration, research on these deficits is equivocal, with some studies showing significant impairment and others suggesting minimal deficits. As such, the present study sought to examine the relationship between laboratory-induced pain and performance on the Paced Auditory Serial Addition Test (PASAT) using a mixed factorial design. Seventy-two nonclinical volunteers were randomly assigned to a pain group, who took the PASAT while experiencing cold pressor-induced pain, or a control group, who took the PASAT while experiencing painless room-temperature water immersion. To account for practice effects, all participants were administered 1 practice trial and 3 standard trials of the PASAT, with the final trial administered in cold pressor-induced pain or painless water immersion. The results revealed a significant interaction between condition and PASAT performance, F(l, 64) = 23.63, ^<.001, partial r2 = 21. The control group increased performance by 6 items while the pain group showed no such improvement. The results suggest that because the pain group did not demonstrate the same practice effects relative to the control group, their performance was impaired by cold pressor-induced pain. However, the impairment was relatively mild (about 0.5 standard deviation) and did not occur in all participants.
机译:尽管临床医生经常观察到患有慢性疼痛的患者经历与记忆力和注意力集中有关的认知缺陷,但是对这些缺陷的研究却模棱两可,有些研究显示明显的损伤,而另一些研究则提示最小的缺陷。因此,本研究试图使用混合因子设计来检查实验室听觉疼痛与听觉连续加法试验(PASAT)的表现之间的关系。 72名非临床志愿者被随机分为一个疼痛组,他们在遭受冷压引起的疼痛时服用了PASAT,或者被分为对照组,他们在无痛的室温水中浸泡时服用了PASAT。为了说明实践效果,对所有参与者进行了1项PASAT的实践试验和3项标准试验,最终试验以冷压诱发的疼痛或无痛浸入水中进行。结果显示,条件与PASAT表现之间存在显着的相互作用,F(l,64)= 23.63,^ <。001,部分r 2 =21。对照组的表现提高了6项,而疼痛组没有表现出这种改善。结果表明,由于疼痛组没有表现出与对照组相同的练习效果,因此冷压引起的疼痛会削弱其性能。但是,损伤相对较轻(约0.5个标准差),并非在所有参与者中都出现。

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