Couturier Jennifer, Nicula Maria, Webb Cheryl, Dimitropoulos Gina, Obeid Nicole, Kimber Melissa, Loewen Techiya, Coolen Anne Marie, Crews Erica, Jones Shaleen, Tremblay Cendrine, Preskow Wendy, McVey Gail, Wozney Lori
McMaster University, 1200 Main St W, Hamilton, ON, L8N3Z5, Canada.
University of Calgary, Calgary, Canada.
J Eat Disord. 2025 Jul 28;13(1):157. doi: 10.1186/s40337-025-01347-2.
This study describes views on the impact of the COVID-19 pandemic on eating disorder symptoms in youth, as well as the impact on care, and the possibility of peer support as a mitigating strategy from the perspectives of youth and parents with lived experience with eating disorders, as well as clinicians and administrators.
A national purposive sample was recruited through websites and social media platforms. Those recruited were asked to complete a demographic questionnaire and to partake in an individual, virtual, semi-structured qualitative interview. Guided by a qualitative descriptive approach, interview data was transcribed and analyzed using qualitative content analysis.
Fifteen parents (93% female; age 48.9 6.9 years), 14 youth (93% female; age 15.3 1.2 years), 16 clinicians (93.8% female; age 41.19 15.7) and 12 administrators (83.3% female; age 47.75 12.2 years) participated. Thirteen parents (87%) said they would attend a parent peer support group and all 15 (100%) said it should be offered routinely in community and hospital settings delivering eating disorder care. Benefits and risks were discussed by participants. Youth, clinicians and administrators agreed that parental peer support groups would be helpful but were not as convinced that youth peer support groups would be beneficial to youth with eating disorders.
Those with lived experience view parental peer support as beneficial and feel it should be offered routinely. Clinicians and administrators also voiced support for parental peer support with certain caveats regarding training and oversight.
The online version contains supplementary material available at 10.1186/s40337-025-01347-2.
本研究描述了从患有饮食失调症的青少年及其父母、临床医生和管理人员的角度,探讨新冠疫情对青少年饮食失调症状的影响、对护理的影响,以及同伴支持作为一种缓解策略的可能性。
通过网站和社交媒体平台招募了一个全国性的有目的样本。被招募者被要求填写一份人口统计问卷,并参加一次个人的、虚拟的、半结构化的定性访谈。在定性描述方法的指导下,对访谈数据进行转录,并使用定性内容分析进行分析。
15名家长(93%为女性;年龄48.9±6.9岁)、14名青少年(93%为女性;年龄15.3±1.2岁)、16名临床医生(93.8%为女性;年龄41.19±15.7岁)和12名管理人员(83.3%为女性;年龄47.75±12.2岁)参与了研究。13名家长(87%)表示他们会参加家长同伴支持小组,所有15名家长(100%)表示应该在提供饮食失调护理的社区和医院环境中定期提供该小组。参与者讨论了益处和风险。青少年、临床医生和管理人员一致认为家长同伴支持小组会有帮助,但对于青少年同伴支持小组对患有饮食失调症的青少年是否有益并不那么确信。
有亲身经历的人认为家长同伴支持是有益的,并认为应该定期提供。临床医生和管理人员也表示支持家长同伴支持,但对培训和监督有一定的保留意见。
在线版本包含可在10.1186/s40337-025-01347-2获取的补充材料。