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在一项大型基于人群的现场研究中测量日间皮质醇浓度的挑战。

Challenges of measuring diurnal cortisol concentrations in a large population-based field study.

机构信息

Department of Maternal and Child Health, University of North Carolina at Chapel Hill (UNC-CH), Chapel Hill, NC, USA.

出版信息

Psychoneuroendocrinology. 2012 Apr;37(4):499-508. doi: 10.1016/j.psyneuen.2011.07.019. Epub 2011 Aug 20.

Abstract

OBJECTIVES

Longitudinal examinations of associations between daily stress, diurnal cortisol concentrations, and physiological parameters in population-based studies are needed. This study evaluates issues related to consent, collection, and protocol adherence for a low-burden saliva collection protocol.

METHODS

In the 2007 pretest (n=193) for Wave IV of the National Longitudinal Study of Adolescent Health (Add Health) a three-sample, one-day, unsupervised saliva collection protocol was pilot tested. Embedded experiments allowed for examination of adherence and effects of monetary incentives.

RESULTS

Although most (97%) study participants consented to collection, only about 80% actually mailed back samples. Use of a time-stamping TrackCap allowed comparison of self-reported and stamp-recorded collection times. Of returned samples, self-report of collection time was missing for about a quarter, and only about one in three respondents (of those for whom adherence was calculable) fully adhered to the collection protocol, indicating significant potential for bias. Consent, return, and protocol adherence were unrelated to key sociodemographic characteristics, and did not improve with higher monetary incentives or knowledge of being monitored.

CONCLUSIONS

Despite the relatively low-burden collection protocol and use of multiple strategies thought to improve collection and protocol adherence, response and adherence were poor, leading to a decision to drop cortisol measurement from the Wave IV Add Health protocol. Large field studies should carefully evaluate the feasibility of collection and protocol adherence for unsupervised collection protocols before implementing costly, and potentially unusable, biological measurements.

摘要

目的

需要对基于人群的研究中日常压力、日间皮质醇浓度与生理参数之间的关联进行纵向研究。本研究评估了一项低负担唾液采集方案在同意、采集和遵守方案方面的相关问题。

方法

在青少年健康纵向研究(Add Health)第四波的 2007 年预测试(n=193)中,对三样本、一日、非监督唾液采集方案进行了试点测试。嵌入式实验允许检查遵守情况和金钱奖励的影响。

结果

尽管大多数(97%)研究参与者同意采集,但只有约 80%的参与者实际邮寄回样本。使用时间戳跟踪帽(Time-stamping TrackCap)可以比较自我报告和盖章记录的采集时间。在返回的样本中,约四分之一的样本自我报告的采集时间缺失,只有大约三分之一的(可计算遵守情况的)受访者完全遵守了采集方案,表明存在显著的偏差风险。同意、返回和遵守与关键社会人口特征无关,并且不会因金钱奖励或被监测的知识而提高。

结论

尽管采集方案负担相对较低,并且使用了多种策略来提高采集和遵守方案的效果,但反应和遵守情况很差,这导致了从第四波 Add Health 协议中删除皮质醇测量的决定。大型现场研究应在实施昂贵且可能无法使用的生物测量之前,仔细评估非监督采集方案的采集和遵守方案的可行性。

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