The Louis Dundas Centre for Children's Palliative Care, University College London Great Ormond Street Institute of Child Health, London, UK.
School of Nursing and Midwifery, Monash University, Melbourne, Australia.
BMC Palliat Care. 2018 Nov 7;17(1):122. doi: 10.1186/s12904-018-0375-4.
As understandings of the impacts of end-of-life experiences on parents' grief and bereavement increase, so too does the inclusion of bereaved parents into research studies exploring these experiences. However, designing and obtaining approval for these studies can be difficult, as guidance derived from bereaved parents' experiences of the research process are limited within the current literature.
We aimed to explore bereaved parents' experiences of research participation in a larger grounded theory study exploring experiences of the death of a child in the paediatric intensive care unit. Data were obtained during follow-up phone calls made to 19 bereaved parents, five of whom provided data from their spouse, 1 week after their participation in the study. Participants were asked to reflect on their experiences of research participation, with a focus on recruitment methods, timing of research contact, and the location of their interview. Parents' responses were analysed using descriptive content analysis.
Our findings demonstrate that despite being emotionally difficult, parents' overall experiences of research participation were positive. Parents preferred to be contacted initially via a letter, with an opt in approach viewed most favourably. Most commonly, participants preferred that research contact occurred within 12-24 months after their child's death, with some suggesting contact after 6 months was also appropriate. Parents also preferred research interviews conducted in their own homes, though flexibility and parental choice was crucial.
Findings from this study offer further insight to researchers and research review committees, to help ensure that future studies are conducted in a way that best meets the unique needs of bereaved parents participating in research.
随着人们对临终体验对父母悲痛和丧亲的影响的理解不断加深,将丧亲父母纳入研究这些体验的研究中也越来越多。然而,设计和获得这些研究的批准可能很困难,因为当前文献中对丧亲父母对研究过程的体验的指导有限。
我们旨在通过一项更大的扎根理论研究来探讨丧亲父母的研究参与体验,该研究探讨了儿科重症监护病房中儿童死亡的体验。在对 19 名丧亲父母进行后续电话访谈时获得了数据,其中 5 名父母的配偶在参与研究后 1 周提供了数据。要求参与者反思他们的研究参与体验,重点是招募方法、研究联系的时间和访谈地点。使用描述性内容分析对父母的回答进行分析。
我们的研究结果表明,尽管情感上很困难,但父母对研究参与的总体体验是积极的。父母更喜欢最初通过信件联系,首选采用选择加入的方法。大多数参与者希望在孩子去世后 12-24 个月内进行研究联系,一些人还建议在 6 个月后进行联系也合适。父母也希望在家中进行研究访谈,但灵活性和父母的选择至关重要。
这项研究的结果为研究人员和研究审查委员会提供了更多的见解,以帮助确保未来的研究以最符合参与研究的丧亲父母独特需求的方式进行。