Zaidi Maryum, Gazarian Priscilla, Mattie Heather, Sheldon Lisa Kennedy, Gakumo C Ann
Solomont School of Nursing, Zuckerberg College of Health Sciences, University of Massachusetts Lowell, Lowell, MA, United States.
Manning College of Nursing & Health Sciences, University of Massachusetts Boston, Boston, MA, United States.
JMIR Aging. 2023 Oct 20;6:e44777. doi: 10.2196/44777.
Despite the role of health information technology (HIT) in patient engagement processes and government incentives for HIT development, research regarding HIT is lacking among older adults with a high burden of chronic diseases such as cancer. This study examines the role of selected sociodemographic factors and cancer-related fatalistic beliefs on patient engagement expressed through HIT use for patient engagement in adults aged ≥65 years. We controlled for cancer diagnosis to account for its potential influence on patient engagement.
This study has 2 aims: to investigate the role of sociodemographic factors such as race, education, poverty index, and psychosocial factors of cancer fatalistic beliefs in accessing and using HIT in older adults and to examine the association between access and use of HIT in the self-management domain of patient activation that serves as a precursor to patient engagement.
This is a secondary data analysis of a subset of the Health Information National Trend Survey (Health Information National Trend Survey 4, cycle 3). The subset included individuals aged ≥65 years with and without a cancer diagnosis. The relationships between access to and use of HIT to several sociodemographic variables and psychosocial factors of fatalistic beliefs were analyzed. Logistic and linear regression models were fit to study these associations.
This study included 180 individuals aged ≥65 years with a cancer diagnosis and 398 without a diagnosis. This analysis indicated that having less than a college education level (P=<.001), being an individual from an ethnic and minority group (P=<.001), and living in poverty (P=.001) were significantly associated with decreased access to HIT. Reduced HIT use was associated with less than a college education (P=.001) and poverty(P=.02). This analysis also indicated that fatalistic beliefs about cancer were significantly associated with lower HIT use (P=.03). Specifically, a 1-point increase in the cancer fatalistic belief score was associated with a 36% decrease in HIT use. We found that controlling for cancer diagnosis did not affect the outcomes for sociodemographic variables or fatalistic beliefs about cancer. However, patients with access to HIT had a self-management domain of patient activation (SMD) score of 0.21 points higher (P=.003) compared with patients who did not have access. SMD score was higher by 0.28 points (P=.002) for individuals who used HIT and 0.14 points higher (P=.04) who had a prior diagnosis of cancer.
Sociodemographic factors (education, race, poverty, and cancer fatalistic beliefs) impact HIT access and use in older adults, regardless of prior cancer diagnosis. Among older adults, HIT users report higher self-management, which is essential for patient activation and engagement.
尽管健康信息技术(HIT)在患者参与过程中发挥着作用,且政府也对HIT的发展给予了激励,但在患有诸如癌症等慢性病负担较重的老年人中,关于HIT的研究却很匮乏。本研究探讨了选定的社会人口学因素和与癌症相关的宿命论信念对≥65岁成年人通过使用HIT进行患者参与所表达的患者参与度的作用。我们对癌症诊断进行了控制,以考虑其对患者参与度的潜在影响。
本研究有两个目标:调查种族、教育程度、贫困指数等社会人口学因素以及癌症宿命论信念等心理社会因素在老年人获取和使用HIT方面的作用,并检验在作为患者参与度先兆的患者激活自我管理领域中,获取和使用HIT之间的关联。
这是对健康信息国家趋势调查(健康信息国家趋势调查4,第3轮)一个子集的二次数据分析。该子集包括有和没有癌症诊断的≥65岁的个体。分析了获取和使用HIT与几个社会人口学变量以及宿命论信念心理社会因素之间的关系。采用逻辑回归和线性回归模型来研究这些关联。
本研究纳入了180名有癌症诊断的≥65岁个体和398名无癌症诊断的个体。该分析表明,教育程度低于大学水平(P<0.001)、属于少数族裔群体(P<0.001)以及生活贫困(P = 0.001)与获取HIT的机会减少显著相关。HIT使用减少与教育程度低于大学水平(P = 0.001)和贫困(P = 0.02)有关。该分析还表明,对癌症的宿命论信念与较低的HIT使用显著相关(P = 0.03)。具体而言,癌症宿命论信念得分每增加1分,HIT使用就减少36%。我们发现,控制癌症诊断并不影响社会人口学变量或对癌症的宿命论信念的结果。然而,与无法获取HIT的患者相比,能够获取HIT的患者在患者激活自我管理领域(SMD)的得分高0.21分(P = 0.003)。使用HIT的个体的SMD得分高0.28分(P = 0.002),有癌症既往诊断的个体的SMD得分高0.14分(P = 0.04)。
社会人口学因素(教育程度、种族、贫困和癌症宿命论信念)会影响老年人获取和使用HIT,无论其是否有癌症既往诊断。在老年人中,HIT使用者报告的自我管理水平更高,这对患者激活和参与至关重要。