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Women's experiences of participating in the Magpie Trial: a postal survey in the United Kingdom.

机译:妇女参加喜p审判的经历:英国的一项邮政调查。

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BACKGROUND: The Magpie Trial compared magnesium sulfate with placebo for women with preeclampsia. The objective of this study was to explore women's views and experiences of participating in the Magpie Trial in the United Kingdom. METHODS: Postal questionnaires were sent to 771 women participants in the Magpie Trial to assess long-term health of UK women and children. The questionnaire included three questions exploring women's experience of participating in the trial: (a) If time suddenly went backward, and you had to do it all over again, would you agree to participate in the Magpie Trial? (b) Please tell us if there was anything about the Magpie Trial that you think could have been done better; and (c) Please tell us if there was anything about the Magpie Trial, or your experience of joining the trial, that you think was particularly good. RESULTS: Overall, 619 of the 771 women who were sent questionnaires returned them. In response to the three questions: (a) 58 percent (356) of women responded definitely yes, 5 percent (33) "definitely no," and 5 percent (34) "not sure." No clear evidence was shown of a relationship with allocated treatment, although women who responded "probably or definitely no" were more likely to have had side effects from trial treatment. (b) Although 44 percent of women stated that nothing could have been done better, free text suggestions related to content of recruitment information, and its timing, and wanting to know treatment allocation and trial results. c) Women were generally extremely positive about being followed up and receiving trial results. CONCLUSIONS: Women were largely positive about participation in the trial and its follow-up, but still reported ways they believed the study could have been improved, such as more information, given earlier, which also has implications for clinical care.
机译:背景:《喜p试验》比较了先兆子痫妇女的硫酸镁和安慰剂。这项研究的目的是探讨妇女在英国参加the试验的观点和经验。方法:向771名喜p试验中的女性参与者发送了邮政调查表,以评估英国妇女和儿童的长期健康状况。该问卷包括三个问题,探讨了妇女参加该试验的经历:(a)如果时间突然倒退,而您又必须重新做一次,您是否同意参加the试验? (b)请告诉我们您是否认为可以做得更好的有关喜p审判的事情; (c)请告诉我们有关喜p审判的事情,或者您参加审判的经验,认为您认为特别好。结果:总体上,在771位被发送问卷的女性中,有619位返回了他们。在回答三个问题时:(a)58%(356)的女性回答肯定是,5%(33)的回答是“肯定”,5%(34)的回答是“不确定”。尽管有“可能或绝对没有”反应的妇女更有可能因试验治疗而产生副作用,但没有明确证据表明与分配的治疗有关系。 (b)尽管有44%的妇女表示无法做得更好,但有关招聘信息内容,时间安排以及想要了解治疗分配和试验结果的免费文本建议。 c)妇女通常对随访和接受试验结果非常积极。结论:妇女对参与该试验及其后续行动的评价总体上是积极的,但仍报告她们认为该研究可以得到改善的方式,例如,较早提供的更多信息,这也对临床护理产生了影响。

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