Group Psychological Treatment Preferences of Individuals Living With Chronic Disease: Brief Report of a Saskatchewan-Based Cross-Sectional Survey.

IF 1.7 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Inquiry-The Journal of Health Care Organization Provision and Financing Pub Date : 2024-01-01 DOI:10.1177/00469580241237112
Kelsey M Haczkewicz, Taylor Hill, Courtney D Cameron, Zona Iftikhar, Natasha L Gallant
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Abstract

Given that individuals with chronic diseases comorbid with psychological distress experience worse clinical outcomes than those without psychological distress, treatment of the psychological sequalae that accompanies chronic diseases is of utmost importance. Thus, the present study aimed to examine group treatment preferences among adults living with chronic disease in Saskatchewan, Canada. An online survey regarding group treatment preferences was administered to 207 participants living with chronic disease comorbid with psychological distress. The most often reported treatment scenario was virtual sessions (45%) lasting 1 h (51%) and occurring every other week (45%) in the evening (63%) for 3 to4 months (40%). Preferences included a medium group (48%), a relatively closed group nature (ie, only occasional new members; 44%), and group leadership including at least 1 professional living with chronic disease (54%). Future-oriented (81%), supportive (83%), skill-based (95%), and group discussions (78%) were desired treatment characteristics among participants. Survey results showed clear preferences on treatment content and session logistics. Slight variations exist by gender and age, but a consensus can be identified and act as a preliminary treatment plan. This study contributes to the body of literature on psychological treatment preferences for individuals living with chronic disease by outlining the preferred format and composition of groups according to those with lived experience. Group-based psychological treatment for chronic disease patients should account for these preferences to improve its acceptability and usefulness among patients.

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慢性病患者的团体心理治疗偏好:萨斯喀彻温省跨部门调查简要报告》。
与没有心理困扰的人相比,合并有心理困扰的慢性病患者的临床疗效更差,因此治疗慢性病的心理后遗症至关重要。因此,本研究旨在调查加拿大萨斯喀彻温省成年慢性病患者对集体治疗的偏好。本研究对 207 名患有慢性疾病并伴有心理困扰的参与者进行了关于集体治疗偏好的在线调查。最常见的治疗方案是虚拟疗程(45%),持续 1 小时(51%),每隔一周(45%)在晚上进行(63%),持续 3-4 个月(40%)。偏好包括中等规模的小组(48%)、相对封闭的小组性质(即只有偶尔的新成员;44%)以及小组领导至少包括一名患有慢性疾病的专业人士(54%)。面向未来(81%)、支持性(83%)、以技能为基础(95%)和小组讨论(78%)是参与者所希望的治疗特点。调查结果显示,参与者对治疗内容和疗程安排有明确的偏好。不同性别和年龄的人对治疗内容的偏好略有不同,但可以达成共识,并作为初步的治疗计划。本研究根据慢性病患者的生活经验,概述了他们对小组形式和组成的偏好,为有关慢性病患者心理治疗偏好的文献做出了贡献。针对慢性病患者的团体心理治疗应考虑到这些偏好,以提高其在患者中的可接受性和实用性。
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来源期刊
CiteScore
2.50
自引率
0.00%
发文量
192
审稿时长
>12 weeks
期刊介绍: INQUIRY is a peer-reviewed open access journal whose msision is to to improve health by sharing research spanning health care, including public health, health services, and health policy.
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