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Attitudes and Preferences Toward a Hypothetical Trial of an Internet-Administered Psychological Intervention for Parents of Children Treated for Cancer: Web-Based Survey

机译:基于互联网的针对患癌症的儿童家长的互联网管理的心理干预假设试验的态度和偏爱:基于网络的调查

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Background Clinical trials are often challenged with issues of recruitment and retention. Little is known concerning general attitudes and preferences toward trial design and willingness to participate among parents of children treated for cancer. Furthermore, willingness to participate in internet-administered psychological interventions remains unexplored. In this study, we examined attitudes and preferences of the population regarding study procedures for a hypothetical trial of an internet-administered psychological intervention. In addition, differences in the response rate between modes of study invitation and willingness to engage in internet-administered interventions were examined. Objective The primary objective of this study was to examine attitudes and preferences toward participating in an internet-administrated psychological intervention. The secondary objective was to examine the response rates and help-seeking behavior among parents of children treated for cancer. Methods A cross-sectional, Web-based survey was conducted with parents of children who had completed cancer treatment. This Web-based survey examined self-reported emotional distress, prior help-seeking and receipt of psychological support, past research participation, attitudes toward research, preferences concerning recruitment procedures, and attitudes toward different types of trial design. Results Of all the parents invited, 32.0% (112/350) completed the survey, with no difference in response rate between modes of study invitation (χ21=0.6, P =.45). The majority (80/112, 71.4%) of parents responded that they had experienced past emotional distress. Responses indicated high (56/112, 50.0%) or somewhat high trust in research (51/112, 45.5%), and the majority of parents would accept, or maybe accept, internet-administered psychological support if offered (83/112, 74.1%). In addition, responses showed a preference for postal study invitation letters (86/112, 76.8%), sent by a researcher (84/112, 75.0%) with additional study information provided on the Web via text (81/112, 72.3%) and video (66/112, 58.9%). Overall, parents responded that trials utilizing a waiting list control, active alternative treatment control, or a patient-preference design were acceptable. Conclusions Parents of children treated for cancer appear willing to participate in trials examining internet-administered psychological support. Findings of this study will inform the design of a feasibility trial examining internet-administered psychological support for the population.
机译:背景技术临床试验通常面临招募和保留问题。人们对试验设计的总体态度和偏好以及接受癌症治疗的儿童的父母之间的参与意愿知之甚少。此外,参与互联网管理的心理干预的意愿仍未得到开发。在这项研究中,我们研究了互联网对心理干预进行假设性试验的人群对研究程序的态度和偏好。此外,研究邀请模式和参与互联网管理干预方式的回应率之间的差异。目的本研究的主要目的是研究对参加互联网管理的心理干预的态度和偏好。次要目标是检查接受癌症治疗的儿童的父母的反应率和寻求帮助的行为。方法对完成癌症治疗的孩子的父母进行基于网络的横断面调查。这项基于网络的调查研究了自我报告的情绪困扰,先前的寻求帮助和心理支持,过去的研究参与,对研究的态度,对招聘程序的偏爱以及对不同类型的试验设计的态度。结果在所有被邀请的父母中,有32.0%(112/350)完成了调查,学习邀请方式之间的回应率没有差异(χ21= 0.6,P = .45)。大多数父母(80 / 112,71.4%)回答说,他们曾经经历过情绪困扰。回应显示对研究的信任度很高(56 / 112,50.0%)或较高(51 / 112,45.5%),并且大多数父母会接受或可能接受互联网提供的心理支持(83/112, 74.1%)。此外,回答显示偏爱由研究人员(84/112,75.0%)发送的邮政学习邀请函(86/112,75.0%),并通过文本在网上提供了其他研究信息(81/112,72.3%) )和视频(66 / 112,58.9%)。总体而言,父母回答说,使用等待名单控制,主动替代治疗控制或患者偏好设计的试验是可以接受的。结论接受癌症治疗的儿童的父母似乎愿意参加检查互联网管理的心理支持的试验。这项研究的结果将为设计可行性试验的设计提供参考,该试验研究了互联网管理的人口心理支持。

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