Behavioural Science Institute, Clinical Psychology, Radboud University, Nijmegen, The Netherlands.
Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC, Canada.
Disabil Rehabil. 2021 May;43(9):1279-1286. doi: 10.1080/09638288.2019.1656292. Epub 2019 Sep 14.
Many people with scleroderma rely on peer-led support groups as a coping resource. Reasons for not attending support groups in scleroderma have been investigated only in North American participants. This study assesses reasons for nonattendance in European countries and compares results with previously published North American findings.
The same 21-item survey as used in the North American sample assessed possible reasons for not attending scleroderma support groups. Proportions of items rated or were compared between samples.
Consistent with the North American survey findings ( = 242), the two items most commonly rated as (Very) Important reasons for nonattendance among 228 European participants were (1) already having enough support (57%), and (2) not knowing of any local scleroderma support groups (58%). Compared to North American non-attenders, European patients were significantly more likely to rate not knowing enough about what happens at support groups (46% vs 19%), not having reliable ways to get to meetings (35% vs 17%), and being uncomfortable sharing experiences with a group (22% vs 11%) as (Very) Important reasons for nonattendance.
Improving access to European support groups, providing education about support groups and group leader training may encourage participation.IMPLICATIONS FOR REHABILITATIONRehabilitation professionals might help develop local support groups for people with systemic sclerosis (scleroderma) to address the lack of access to these groups for many patients.The need for transportation and limited local accessibility may also be addressed by implementing online systemic sclerosis support groups.Professionals in the field of rehabilitation may work with people with systemic sclerosis and patient organizations to provide education about support groups to improve support group attendance in Europe.
许多硬皮病患者依赖于同行主导的支持小组作为应对资源。在北美参与者中,仅对不参加硬皮病支持小组的原因进行了调查。本研究评估了欧洲国家不参加的原因,并将结果与之前发表的北美研究结果进行了比较。
使用与北美样本相同的 21 项调查评估了不参加硬皮病支持小组的可能原因。比较了两个样本中评分或的项目比例。
与北美调查结果一致( = 242),228 名欧洲参与者中,两项最常被评为不参加硬皮病支持小组的(非常)重要原因是(1)已经有足够的支持(57%),(2)不知道当地的硬皮病支持小组(58%)。与北美不参加者相比,欧洲患者更有可能将不知道支持小组发生的事情(46%比 19%)、没有可靠的方法参加会议(35%比 17%)以及与小组分享经验感到不舒服(22%比 11%)评为(非常)重要的不参加原因。
改善欧洲支持小组的获取途径,提供有关支持小组的教育和小组领导培训,可能会鼓励患者参加。
康复专业人员可以帮助为患有系统性硬化症(硬皮病)的人建立当地的支持小组,以解决许多患者无法获得这些小组的问题。交通问题和当地有限的可达性也可以通过实施在线系统性硬化症支持小组来解决。康复领域的专业人员可以与系统性硬化症患者和患者组织合作,提供有关支持小组的教育,以提高欧洲的支持小组出勤率。