Delisle Vanessa C, Gumuchian Stephanie T, Pelaez Sandra, Malcarne Vanessa L, El-Baalbaki Ghassan, Körner Annett, Hudson Marie, Baron Murray, Thombs Brett D
Department of Educational and Counselling Psychology, McGill University; and Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada.
Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Québec, Canada.
Clin Exp Rheumatol. 2016 Sep-Oct;34 Suppl 100(5):56-62. Epub 2016 Feb 25.
Peer-led support groups are an important resource for people living with many rare diseases, including scleroderma (systemic sclerosis, SSc). Little is known, however, about the accessibility of SSc support groups and factors that may discourage people from participating in these groups. The objective of this study was to identify reasons why people with SSc do not participate in SSc support groups.
Canadians with SSc were recruited to complete the Canadian Scleroderma Patient Survey of Health Concerns and Research Priorities. Data from respondents who answered the question "Have you participated in SSc support groups?" with "No" were analyzed. Frequencies of participants who responded (1) I'm not interested, (2) None are easily available, and (3) Other (please specify) were tallied. A content analysis approach was used to code the open-ended responses to this question.
A total of 280 respondents provided a reason for non-participation in SSc support groups. Key reasons for not participating in support groups included: (1) Not interested or no perceived need (36%); (2) No local support group available (35%); (3) Lack of awareness of the existence of SSc support groups (13%); (4) Practical barriers (6%); (5) Emotional factors (4%); (6) Uncertainty about whether to attend (4%); and (7) Negative perceptions about support groups (3%).
SSc organizations may be able to address current limitations in the accessibility and effectiveness of SSc support groups by implementing online support groups, as well as by providing support group leaders training to help establish and sustain successful SSc support groups.
同伴主导的支持小组是许多罕见病患者(包括硬皮病,即系统性硬化症,SSc)的重要资源。然而,关于SSc支持小组的可及性以及可能阻碍人们参与这些小组的因素,我们所知甚少。本研究的目的是确定SSc患者不参加SSc支持小组的原因。
招募患有SSc的加拿大人来完成《加拿大硬皮病患者健康关注与研究重点调查问卷》。对回答“你参加过SSc支持小组吗?”问题时回答“没有”的受访者的数据进行分析。统计回答(1)我不感兴趣,(2)没有容易参加的小组,以及(3)其他(请注明)的参与者频率。采用内容分析法对该问题的开放式回答进行编码。
共有280名受访者给出了不参加SSc支持小组的原因。不参加支持小组的主要原因包括:(1)不感兴趣或感觉没有必要(36%);(2)当地没有支持小组(35%);(3)对SSc支持小组的存在缺乏了解(13%);(4)实际障碍(6%);(5)情感因素(4%);(6)不确定是否参加(4%);以及(7)对支持小组的负面看法(3%)。
SSc组织或许可以通过实施在线支持小组,以及为支持小组组长提供培训以帮助建立和维持成功的SSc支持小组,来解决当前SSc支持小组在可及性和有效性方面的局限性。