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首页> 外文期刊>Rheumatology international. >'Exercise to me is a scary word': perceptions of fatigue, sleep dysfunction, and exercise in people with fibromyalgia syndrome-a focus group study
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'Exercise to me is a scary word': perceptions of fatigue, sleep dysfunction, and exercise in people with fibromyalgia syndrome-a focus group study

机译:对我来说,对我来说是一种可怕的词:对患有纤维肌痛综合征的人们的疲劳,睡眠功能障碍和锻炼的看法 - 一个焦点小组研究

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摘要

Fibromyalgia syndrome (FMS) is a common and complex chronic pain condition. Exercise is recommended in the management of the FMS; however, people with FMS often find exercise exacerbates their condition and causes overwhelming fatigue. The objective of this study was to explore the perceptions of fatigue and sleep dysfunction, and exercise in people with FMS. Three, 60-90 min focus groups were conducted with people with FMS (n = 14). Participants were recruited from patient support groups who had experienced therapeutic exercise in the management of their condition. Focus groups were video and audio recorded and transcriptions analysed for thematic content by three independent evaluators. Fatigue, sleep dysfunction, and pain were universally reported by participants. The over-arching theme to emerge was a lack of understanding of the condition by others. A huge sense of loss was a major sub-theme and participants felt that they had fundamentally changed since the onset of FMS. Participants reported that they were unable to carry out their normal activities, including physical activity and exercise. The invisibility of FMS was associated with the lack of understanding by others, the sense of loss, and the impact of FMS. People with FMS perceive that there is a lack of understanding of the condition among health care professionals and the wider society. Those with FMS expressed a profound sense of loss of their former 'self'; part of this loss was the ability to engage in normal physical activity and exercise.
机译:纤维肌痛综合征(FMS)是一种常见而复杂的慢性疼痛状况。在FMS管理中建议锻炼;然而,具有FMS的人通常会发现运动加剧了他们的病情并导致压倒性的疲劳。本研究的目的是探讨疲劳和睡眠功能障碍的看法,并在具有FMS的人们中锻炼身体。三个,60-90分钟的聚焦组与具有FMS的人进行(n = 14)。参与者从患者支持群体招募,他们在管理其状况管理方面经历了治疗运动。焦点小组是视频和音频记录,并通过三个独立评估人员分析主题内容的转录。参与者普遍报告疲劳,睡眠功能障碍和疼痛。出现过度拱起的主题是对他人的病情缺乏了解。巨大的损失感是一个主要的子主题,参与者认为自FMS发病以来他们从根本上改变。与会者报告说,他们无法进行正常活动,包括身体活动和运动。 FMS的隐形与其他人缺乏理解,损失感和FMS的影响有关。有FMS的人们认为,对医疗保健专业人员和更广泛的社会的条件缺乏了解。那些有FMS的人表示了对他们以前的“自我”丧失的一种深刻意义;这种损失的一部分是能够与正常身体活动和运动进行锻炼。

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