以学校为基础的促进英语中学性健康的社会营销干预:积极选择试点集群随机对照试验

R. Ponsford, S. Bragg, E. Allen, N. Tilouche, R. Meiksin, Lucy Emmerson, L. Van Dyck, C. Opondo, S. Morris, J. Sturgess, Elizabeth Brocklehurst, A. Hadley, G. Melendez‐Torres, D. Elbourne, H. Young, M. Lohan, C. Mercer, R. Campbell, C. Bonell
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Setting The south of England: optimisation and feasibility-testing in one secondary school; pilot cluster trial in six other secondary schools (four intervention, two control) varying by local deprivation and educational attainment. Participants School students in year 8 at baseline, and school staff. Interventions Schools were randomised (1 : 2) to control or intervention. The intervention comprised staff training, needs survey, school health promotion council, year 9 curriculum, student-led social marketing, parent information and review of school/local sexual health services. Main outcome measures The prespecified criteria for progression to Phase III concerned intervention fidelity of delivery and acceptability; successful randomisation and school retention; survey response rates; and feasible linkage to routine administrative data on pregnancies. The primary health outcome of births was assessed using routine data on births and abortions, and various self-reported secondary sexual health outcomes. Data sources The data sources were routine data on births and abortions, baseline and follow-up student surveys, interviews, audio-recordings, observations and logbooks. Results The intervention was optimised and feasible in the first secondary school, meeting the fidelity targets other than those for curriculum delivery and criteria for progress to the pilot trial. In the pilot trial, randomisation and school retention were successful. Student response rates in the intervention group and control group were 868 (89.4%) and 298 (84.2%), respectively, at baseline, and 863 (89.0%) and 296 (82.0%), respectively, at follow-up. The target of achieving ≥ 70% fidelity of implementation of essential elements in three schools was achieved. 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引用次数: 7

摘要

英国仍然是西欧青少年生育率最高的国家。青少年也是最容易经历意外怀孕的年龄组,大约有一半的人在这个年龄段怀孕。目标是优化和可行性测试积极选择,然后在英格兰南部进行试点试验,评估是否根据预先规定的标准进入第三阶段是合理的。设计干预优化及可行性测试;随机对照试验。英格兰南部:一所中学的优化与可行性测试在其他六所中学(四所干预,两所对照)进行的试点集群试验因当地贫困和教育程度而异。参与者基线为八年级学生和学校工作人员。干预措施学校随机分为对照和干预两组(1:2)。干预措施包括员工培训、需求调查、学校健康促进委员会、九年级课程、学生主导的社会营销、家长信息和学校/地方性健康服务审查。进入第三阶段的预先规定的标准涉及干预的交付保真度和可接受性;成功的随机化和学校保留率;调查回应率;以及与常规怀孕管理数据的可行联系。使用关于分娩和堕胎的常规数据以及各种自我报告的次要性健康结果来评估分娩的主要健康结果。数据来源包括出生和堕胎的常规数据、基线和随访学生调查、访谈、录音、观察和日志。结果该干预措施在第一中学得到了优化和可行,满足了除课程交付外的保真度指标和试点进展标准。在试点试验中,随机化和学校保留是成功的。干预组和对照组的学生反应率基线时分别为868(89.4%)和298(84.2%),随访时分别为863(89.0%)和296(82.0%)。三所学校基本要素实施保真度达到≥70%的目标。关系和性教育主题的覆盖率在干预学校比对照学校高得多。80%的学生接受了这种干预。对工作人员的采访表明,他们很容易接受。数据链接是可行的,但在我们的队列中没有出生或流产的精确匹配。措施表现良好。在一些性行为测量上,较差的重测信度反映出这是一群发育中的青少年。定性研究证实了干预和变革理论的适当性,但提出了一些改进意见。优化学校经历了领导层的反复更迭,这削弱了它的参与。没有进行慢化剂分析,因为这些分析的动力非常不足。结论:我们的研究结果表明,这种干预措施已经达到了进入III期试验的预定标准。青少年怀孕率的下降表明,全面试验的主要结果可以被更全面的性健康指标所取代。任何未来的III期试验都应该有更长的时间从随机化到干预开始。当前对照试验ISRCTN12524938。该项目由国家卫生研究所(NIHR)公共卫生研究方案资助,将全文发表在《公共卫生研究》上;第9卷第1期请参阅NIHR期刊图书馆网站了解更多项目信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A school-based social-marketing intervention to promote sexual health in English secondary schools: the Positive Choices pilot cluster RCT
Background The UK still has the highest rate of teenage births in western Europe. Teenagers are also the age group most likely to experience unplanned pregnancy, with around half of conceptions in those aged Objectives To optimise and feasibility-test Positive Choices and then conduct a pilot trial in the south of England assessing whether or not progression to Phase III would be justified in terms of prespecified criteria. Design Intervention optimisation and feasibility testing; pilot randomised controlled trial. Setting The south of England: optimisation and feasibility-testing in one secondary school; pilot cluster trial in six other secondary schools (four intervention, two control) varying by local deprivation and educational attainment. Participants School students in year 8 at baseline, and school staff. Interventions Schools were randomised (1 : 2) to control or intervention. The intervention comprised staff training, needs survey, school health promotion council, year 9 curriculum, student-led social marketing, parent information and review of school/local sexual health services. Main outcome measures The prespecified criteria for progression to Phase III concerned intervention fidelity of delivery and acceptability; successful randomisation and school retention; survey response rates; and feasible linkage to routine administrative data on pregnancies. The primary health outcome of births was assessed using routine data on births and abortions, and various self-reported secondary sexual health outcomes. Data sources The data sources were routine data on births and abortions, baseline and follow-up student surveys, interviews, audio-recordings, observations and logbooks. Results The intervention was optimised and feasible in the first secondary school, meeting the fidelity targets other than those for curriculum delivery and criteria for progress to the pilot trial. In the pilot trial, randomisation and school retention were successful. Student response rates in the intervention group and control group were 868 (89.4%) and 298 (84.2%), respectively, at baseline, and 863 (89.0%) and 296 (82.0%), respectively, at follow-up. The target of achieving ≥ 70% fidelity of implementation of essential elements in three schools was achieved. Coverage of relationships and sex education topics was much higher in intervention schools than in control schools. The intervention was acceptable to 80% of students. Interviews with staff indicated strong acceptability. Data linkage was feasible, but there were no exact matches for births or abortions in our cohort. Measures performed well. Poor test–retest reliability on some sexual behaviour measures reflected that this was a cohort of developing adolescents. Qualitative research confirmed the appropriateness of the intervention and theory of change, but suggested some refinements. Limitations The optimisation school underwent repeated changes in leadership, which undermined its participation. Moderator analyses were not conducted as these would be very underpowered. Conclusion Our findings suggest that this intervention has met prespecified criteria for progression to a Phase III trial. Future work Declining prevalence of teenage pregnancy suggests that the primary outcome in a full trial could be replaced by a more comprehensive measure of sexual health. Any future Phase III trial should have a longer lead-in from randomisation to intervention commencement. Trial registration Current Controlled Trials ISRCTN12524938. Funding This project was funded by the National Institute for Health Research (NIHR) Public Health Research programme and will be published in full in Public Health Research ; Vol. 9, No. 1. See the NIHR Journals Library website for further project information.
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