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Effects of pain on cognitive function and mobility

机译:疼痛对认知功能和活动性的影响

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Background: Chronic pain has been associated with impaired cognitive function as well as limitations in physical mobility in older adults. This study was conducted to determine whether acute pain that is typically self-diagnosed and self-treated with nonprescription analgesics also affects cognitive function or mobility. Methods: In this placebo-controlled, randomized study, generally healthy adults with recurrent acute joint, back, head, or menstrual pain underwent assessments of cognitive function (Axon Sports Priming Application, Cambridge Neuropsychological Test Automated Battery) and mobility (gait, time to stand, and grip force) during pain (≥5 out of 10 on Brief Pain Inventory – Short Form Q6) vs after pain resolution. Assessments during pain were made before and after treatment with paracetamol 500 mg, paracetamol 500 mg/caffeine 65 mg, or placebo. Primary and secondary outcomes, respectively, were the effects of pain on cognition and mobility vs the pain-free state. The effects of nonprescription analgesics on these outcomes were intended as an exploratory outcome but were not analyzed due to early termination of the study for breaches of Good Clinical Practice guidelines. Results: At termination, 54 individuals had been screened and 21 randomized (safety population). The primary analysis population (modified intent-to-treat) consisted of 20 participants with no inclusion/exclusion violations. Due to early termination, the study did not meet prespecified recruitment levels; therefore, no conclusions could be drawn regarding the effects of pain on cognitive performance or mobility. There were three treatment-emergent adverse events (placebo: reflux disease and hypercholesterolemia; paracetamol: pharyngeal erythema). Conclusion: Because the study was terminated before reaching prespecified recruitment levels, conclusions cannot be drawn regarding the effects of pain or relief from pain by analgesics on cognition or mobility. However, the methodology can serve as a model for addressing these important questions in future investigations. Safety results were consistent with the safety profile for nonprescription paracetamol and paracetamol/caffeine.
机译:背景:慢性疼痛与老年人认知功能受损以及身体活动受限有关。进行这项研究是为了确定通常由非处方镇痛药自我诊断和自我治疗的急性疼痛是否也会影响认知功能或活动能力。方法:在这项安慰剂对照的随机研究中,对患有复发性急性关节,背部,头部或月经痛的一般健康成年人进行了认知功能(Axon Sports Priming Application,Cambridge Neuropsychological Test Automated Battery)和活动能力(步态,运动时间)的评估疼痛期间(站立疼痛量表中的Q5-简短表格Q6中,满分10分中的5分以上)与疼痛缓解后的情况。在对乙酰氨基酚500 mg,对乙酰氨基酚500 mg /咖啡因65 mg或安慰剂治疗之前和之后进行疼痛评估。主要结果和次要结果分别是疼痛对认知和活动的影响与无痛状态的关系。非处方镇痛药对这些结局的影响意在作为探索性结局,但由于该研究因违反《良好临床实践》准则而提前终止研究,因此未进行分析。结果:终止时,已经筛选了54位个体,并随机分配了21位(安全人群)。主要分析人群(改良的意向治疗)由20名参与者组成,没有违反纳入/排除规定。由于提前终止,该研究未达到预定的招募水平;因此,无法得出关于疼痛对认知能力或活动能力的影响的结论。出现了三种治疗急救不良事件(安慰剂:反流病和高胆固醇血症;对乙酰氨基酚:咽部红斑)。结论:由于该研究在达到预定的招募水平之前就已终止,因此无法就止痛药对认知或活动性的疼痛或缓解疼痛的影响得出结论。但是,该方法学可以作为在将来的调查中解决这些重要问题的模型。安全性结果与非处方对乙酰氨基酚和扑热息痛/咖啡因的安全性一致。

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