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“When it goes back to my normal I suppose”: a qualitative study using online focus groups to explore perceptions of ‘control’ amongst people with eczema and parents of children with eczema in the UK

机译:“我想我应该恢复正常了”:一项定性研究,使用在线焦点小组探讨了英国湿疹患者和湿疹儿童父母对“控制”的看法

摘要

Objective: To inform the development of a core outcome set for eczema by engaging with people with eczema and parents of children with eczema to understand their experiences and understanding of the concept “eczema control”.udDesign: 37 participants took part in a total of 6 semi-structured online focus groups held in a typed chatroom with 5-7 participants per group. Three groups involved adults with eczema and three groups involved parents of children with eczema. Framework analysis was used for data analysis.udSetting: A community-based sample was recruited from across the UK via social media and email.udParticipants: 19 adults aged 17-61 (15/19 female, 16/19 white) and 18 parents of children with eczema aged 9 months-17 years (9/18 female, 18/19 white).udResults: Four main themes were identified. 1) “Commonalities and differences in the experiences of control”: a reduction in symptoms such as itch and sleep loss characterised eczema control, but what level was acceptable differed across participants. 2) “Eczema control goes beyond the skin”: psychological factors, social factors, the constant scratching and the impact on everyday activities are a variety of ways an individual can be impacted. 3) “Stepping up and down of treatment”: participants’ stepped-up treatment in response to loss of control, but several factors complicated this behaviour. Control needed to be maintained after stepped-up treatment ended to be acceptable. 4) “How to measure control”: self-report was generally preferred to allow frequent measurements and to capture unobservable features. Although most thought their eczema needed to be measured frequently, many also felt that this was not always realistic or desirable.udConclusions: Eczema “control” is a complex experience for people with eczema and parents of children with the condition. These experiences could have important implications on how long-term control should be measured in eczema clinical trials and clinical practice.
机译:目的:通过与湿疹患者和湿疹患儿的父母接触,了解他们的经历和对“湿疹控制”概念的了解,从而为湿疹核心结局的制定提供信息。 udDesign:共有37名参与者参加了6个半结构化在线焦点小组在类型化的聊天室中举行,每小组5-7名参与者。三组涉及湿疹成人,三组涉及湿疹儿童的父母。框架分析用于数据分析。 ud设置:通过社交媒体和电子邮件从英国各地招募了一个基于社区的样本。 ud参与者:19位年龄在17-61岁之间的成年人(15/19位女性,16/19位白人)和18岁9个月至17岁的湿疹儿童父母(女性9/18,白人18/19)。 ud结果:确定了四个主要主题。 1)“控制经验的共同点和差异”:湿疹控制的特征是瘙痒和睡眠不足等症状的减轻,但不同参与者的可接受水平不同。 2)“湿疹控制超出皮肤范围”:心理因素,社会因素,持续的抓挠以及对日常活动的影响是影响个人的多种方式。 3)“加强治疗”:参与者因失去控制而加强治疗,但是有几个因素使这种行为复杂化。逐步接受治疗后需要维持控制。 4)“如何测量控制”:通常建议使用自我报告,以便进行频繁测量并捕获无法观察到的特征。尽管大多数人认为需要经常测量他们的湿疹,但许多人也认为这并不总是现实或可取的。 ud结论:对于患有湿疹的人和患有此病的孩子的父母,湿疹“控制”是一种复杂的经历。这些经验可能对湿疹临床试验和临床实践中应测量的长期控制有重要意义。

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