Edgar Chris J, Siemers Eric, Maruff Paul, Petersen Ronald C, Aisen Paul S, Weiner Michael W, Albala Bruce
Cogstate Ltd, London, UK.
Cogstate Ltd, New Haven, CT, USA.
J Alzheimers Dis. 2021;83(2):915-925. doi: 10.3233/JAD-210201.
There is a need for feasible, scalable assessments to detect cognitive impairment and decline. The Cogstate Brief Battery (CBB) is validated for Alzheimer's disease (AD) and in unsupervised and bring your own device contexts. The CBB has shown usability for self-completion in the home but has not been employed in this way in a multisite clinical trial in AD.
The objective of the pilot was to evaluate feasibility of at-home, self-completion of the CBB in the Alzheimer's Disease Neuroimaging Initiative (ADNI) over 24 months.
The CBB was included as a pilot for cognitively normal (CN) and mild cognitive impairment (MCI) participants in ADNI-2, invited to take the assessment in-clinic, then at at-home over a period of 24 months follow-up. Data were analyzed to explore acceptability/usability, concordance of in-clinic and at-home assessment, and validity.
Data were collected for 104 participants (46 CN, 51 MCI, and 7 AD) who consented to provide CBB data. Subsequent analyses were performed for the CN and MCI groups only. Test completion rates were 100%for both the first in-clinic supervised and first at-home unsupervised assessments, with few repeat performances required. However, available follow-up data declined sharply over time. Good concordance was seen between in-clinic and at-home assessments, with non-significant and small effect size differences (Cohen's d between -0.04 and 0.28) and generally moderate correlations (r = 0.42 to 0.73). Known groups validity was also supported (11/16 comparisons with Cohen's d≥0.3).
These data demonstrate the feasibility of use for the CBB for unsupervised at-home, testing, including MCI groups. Optimal approaches to the application of assessments to support compliance over time remain to be determined.
需要可行的、可扩展的评估方法来检测认知障碍和衰退。Cogstate简版测试组合(CBB)已在阿尔茨海默病(AD)以及无监督和自带设备的环境中得到验证。CBB已显示出在家中自我完成测试的可用性,但尚未在AD的多中心临床试验中以这种方式使用。
该试点研究的目的是评估在阿尔茨海默病神经影像学计划(ADNI)中,24个月内在家中自我完成CBB测试的可行性。
CBB被纳入ADNI-2中认知正常(CN)和轻度认知障碍(MCI)参与者的试点研究,邀请他们先在诊所进行评估,然后在24个月的随访期内在家中进行评估。对数据进行分析,以探讨可接受性/可用性、诊所评估和家庭评估的一致性以及有效性。
收集了104名同意提供CBB数据的参与者(46名CN、51名MCI和7名AD)的数据。随后仅对CN和MCI组进行了分析。首次诊所监督评估和首次家庭无监督评估的测试完成率均为100%,几乎无需重复测试。然而,随着时间的推移,可用的随访数据急剧下降。诊所评估和家庭评估之间存在良好的一致性,差异不显著且效应量较小(Cohen's d在-0.04至0.28之间),相关性一般为中等(r = 0.42至0.73)。已知组有效性也得到了支持(16项比较中有11项Cohen's d≥0.3)。
这些数据证明了CBB用于无监督家庭测试的可行性,包括MCI组。随着时间的推移,支持依从性的评估应用的最佳方法仍有待确定。