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用于指导高血压患者干预措施个性化定制的心理行为特征:潜在特征分析

Psychobehavioral Profiles to Assist Tailoring of Interventions for Patients With Hypertension: Latent Profile Analysis.

作者信息

Tanaka Rika, Nolan Robert P

机构信息

Cardiac eHealth and Behavioural Cardiology Research Unit, Peter Munk Cardiac Centre, University Health Network, Toronto, ON, Canada.

Department of Psychiatry and Institute of Medical Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

出版信息

J Med Internet Res. 2018 May 11;20(5):e149. doi: 10.2196/jmir.8757.

Abstract

BACKGROUND

Practice guidelines advocate combining pharmacotherapy with lifestyle counseling for patients with hypertension. To allow for appropriate tailoring of interventions to meet individual patient needs, a comprehensive understanding of baseline patient characteristics is essential. However, few studies have empirically assessed behavioral profiles of hypertensive patients in Web-based lifestyle counseling programs.

OBJECTIVE

The objectives of this study were to (1) specify baseline psychobehavioral profiles of patients with hypertension who were enrolled in a Web-based lifestyle counseling trial, and (2) examine mean differences among the identified profile groups in demographics, psychological distress, self-reported self-care behaviors, physiological outcomes, and program engagement to determine prognostic implications.

METHODS

Participants (N=264; mean age 57.5 years; 154/264, 58.3% female; 193/264, 73.1% white) were recruited into a longitudinal, double-blind, randomized controlled trial, designed to evaluate an online lifestyle intervention for hypertensive patients. A series of latent profile analyses identified psychobehavioral profiles, indicated by baseline measures of mood, motivation, and health behaviors. Mean differences between profile groups were then explored.

RESULTS

A 2-class solution provided the best model fit (the Bayesian information criterion (BIC) is 10,133.11; sample-size adjusted BIC is 10,006.54; Lo-Mendell-Rubin likelihood ratio test is 65.56, P=.001). The 2 profile groups were (1) adaptive adjustment, marked by low distress, high motivation, and somewhat satisfactory engagement in health behaviors and (2) affectively distressed, marked by clinically significant distress. At baseline, on average, affectively distressed patients had lower income, higher body mass index, and endorsed higher stress compared with their adaptive adjustment counterparts. At 12-months post intervention, treatment effects were sustained for systolic blood pressure and Framingham risk index in the adaptive adjustment group, and those in the adaptive adjustment group were 2.4 times more likely to complete the 12-month intervention study, compared with their affectively distressed counterparts.

CONCLUSIONS

Interventions for patients who are adaptively adjusted may differ in focus from those designed for the affectively distressed patients. As such, this study underscores the importance of identifying psychobehavioral profiles, as they allow for evidence-based tailoring of lifestyle counseling programs for patients with hypertension.

TRIAL REGISTRATION

ClinicalTrials.gov NCT01541540; https://clinicaltrials.gov/ct2/show/NCT01541540 (Archived by WebCite at http://www.webcitation.org/6yzZYZcWF).

摘要

背景

实践指南提倡对高血压患者将药物治疗与生活方式咨询相结合。为了能够根据个体患者需求进行适当的干预调整,全面了解患者的基线特征至关重要。然而,很少有研究实证评估基于网络的生活方式咨询项目中高血压患者的行为特征。

目的

本研究的目的是:(1)明确参加基于网络的生活方式咨询试验的高血压患者的基线心理行为特征;(2)检查已识别的特征组在人口统计学、心理困扰、自我报告的自我护理行为、生理结果和项目参与度方面的平均差异,以确定预后意义。

方法

参与者(N = 264;平均年龄57.5岁;154/264,58.3%为女性;193/264,73.1%为白人)被招募进入一项纵向、双盲、随机对照试验,该试验旨在评估针对高血压患者的在线生活方式干预。一系列潜在特征分析确定了心理行为特征,这些特征由情绪、动机和健康行为的基线测量指标表示。然后探讨了特征组之间的平均差异。

结果

一个两类解决方案提供了最佳的模型拟合(贝叶斯信息准则(BIC)为10,133.11;样本量调整后的BIC为10,006.54;洛 - 门德尔 - 鲁宾似然比检验为65.56,P = 0.001)。这两个特征组分别是:(1)适应性调整组,其特征为低困扰、高动机以及在健康行为方面的参与度较为令人满意;(2)情感困扰组,其特征为具有临床上显著的困扰。在基线时,平均而言,情感困扰的患者与适应性调整的患者相比,收入较低、体重指数较高且承受的压力更大。在干预后的12个月,适应性调整组的收缩压和弗雷明汉风险指数的治疗效果得以持续,并且与情感困扰的患者相比。适应性调整组的患者完成12个月干预研究的可能性是情感困扰组患者的2.4倍。

结论

针对适应性调整患者的干预措施在重点上可能与针对情感困扰患者的不同。因此,本研究强调了识别心理行为特征的重要性,因为这有助于为高血压患者基于证据地定制生活方式咨询项目。

试验注册

ClinicalTrials.gov NCT01541540;https://clinicaltrials.gov/ct2/show/NCT01541540(由WebCite存档于http://www.webcitation.org/6yzZYZcWF)

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