Clinical and cost-effectiveness of parenting intervention for mothers experiencing psychosocial stress: insights from the early closure of the Mellow Babies RCT.

Lucy Thompson, Jessica Tanner, Matthew Breckons, Naomi Young, Laura Ternent, Thenmalar Vadiveloo, Philip Wilson, Danny Wight, Louise Marryat, Iain McGowan, Graeme MacLennan, Angus MacBeth, James McTaggart, Tim Allison, John Norrie
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引用次数: 0

Abstract

Background: Problems in children's early social and emotional development are likely to have major long-term consequences for the individual and society: maternal emotional well-being is associated with better outcomes. Interventions designed to improve both maternal mental health and the mother-child relationship are thus likely to benefit both maternal health and child development.

Objectives: To establish the clinical and cost-effectiveness of the Mellow Babies parenting intervention for women experiencing psychosocial stress and their 6- to 18-month-old babies. Secondary aims included understanding the process of recruitment, retention and engagement in both the trial and the intervention.

Design: This was a single-centre randomised controlled trial, employing 1 : 1 randomisation with participants allocated to receive Mellow Babies plus usual care, or usual care only.

Setting: Community settings in the Highland Council region of Scotland.

Participants: We aimed to recruit 212 mothers to provide evaluable data for 170 participants (90% power to detect an effect size of 0.5 for the primary outcome). Eligible mothers lived within the Highland Council region; were aged ≥ 16 years; had primary caregiving responsibility of a baby aged 6-18 months and scored above threshold for anxiety (≥ 11) and/or depression (≥ 7) on the Hospital Anxiety and Depression Scale.

Intervention: Mellow Babies is a 14-week group-based parenting programme specifically designed for mothers with psychosocial difficulties. Sessions run for 5 hours each and include 4-10 participants.

Main outcome measures: Maternal Hospital Anxiety and Depression Scale scores at 8 months post randomisation and when the child reaches 30 months. Health economic (service use and quality of life) and child development (language development and mental well-being) outcomes were also examined.

Results: Due to the COVID-19 pandemic, the trial did not recruit to target: 106 women were recruited (53 per arm). It was not possible to explore the clinical and cost-effectiveness of Mellow Babies. Baseline, follow-up and process evaluation data were analysed to allow optimal learning from the study. Direct communication (letter) combined with health visitor referral was a better means of recruitment. Despite relatively low sociodemographic disadvantage, there was a high prevalence of mental ill health. Retention to follow-up and within the intervention was good (75% to study end point), and data were well-completed. Quality-of-life ratings increased at 8 months post randomisation, then decreased somewhat at 30 months of age, but remained above baseline. Qualitative interviews highlighted barriers and facilitators of engagement with the intervention groups. There was no observed difference in baseline characteristics or outcomes between participants recruited before and after the pandemic, although the logistical impact on the trial was profound.

Limitations: The study was not sufficiently powered to answer the main outcome questions. The occurrence of the COVID-19 pandemic severely hampered the current trial.

Conclusions: This trial was not able to answer questions on clinical and cost-effectiveness. Learning from this trial could inform a new re-designed trial including cluster randomisation and based within a larger and more varied population.

Future work: There is still a need for a definitive trial of Mellow Babies. It would likely be most fruitful to conduct a cluster randomised trial, with full buy-in from key health service stakeholders and front-line practitioners, to maximise recruitment, engagement and participation.

Trial registration: The trial is registered as ISRCTN47575326.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Public Health Research programme (NIHR award ref: 15/126/05) and is published in full in Public Health Research; Vol. 12, No. 17. See the NIHR Funding and Awards website for further award information.

对经历心理社会压力的母亲进行育儿干预的临床和成本效益:来自“圆润婴儿”随机对照试验早期结束的见解。
背景:儿童早期社会和情感发展的问题可能对个人和社会产生重大的长期影响:母亲的情感健康与更好的结果相关。因此,旨在改善产妇心理健康和母子关系的干预措施可能有利于产妇健康和儿童发展。目的:探讨“圆润婴儿”育儿干预对经历心理社会压力的妇女及其6 ~ 18个月大的婴儿的临床和成本效益。次要目标包括了解在试验和干预中招募、保留和参与的过程。设计:这是一项单中心随机对照试验,采用1:1随机化,参与者被分配接受“柔和婴儿”加常规护理,或仅接受常规护理。环境:苏格兰高地议会地区的社区环境。参与者:我们的目标是招募212名母亲,为170名参与者提供可评估的数据(90%的能力检测到主要结局的效应量为0.5)。符合条件的母亲居住在高地理事会区域内;年龄≥16岁;对6-18个月的婴儿负有主要照顾责任,并且在医院焦虑和抑郁量表上的焦虑(≥11)和/或抑郁(≥7)得分高于阈值。干预:温柔婴儿是一个为期14周的以团体为基础的育儿计划,专门为有社会心理困难的母亲设计。每节课5小时,包括4-10名参与者。主要结果测量:随机分组后8个月和孩子30个月时的产妇医院焦虑和抑郁量表评分。还检查了健康经济(服务使用和生活质量)和儿童发展(语言发展和心理健康)结果。结果:由于COVID-19大流行,该试验没有招募目标:招募了106名女性(每组53名)。不可能探索“圆润婴儿”的临床和成本效益。基线,随访和过程评估数据进行分析,以便从研究中获得最佳学习。直接沟通(信函)结合卫生访视员推荐是较好的招聘方式。尽管社会人口劣势相对较低,但精神疾病的发病率很高。随访和干预期间的保留率良好(75%至研究终点),数据完整。生活质量评分在随机化后8个月增加,然后在30个月时略有下降,但仍高于基线。定性访谈强调了与干预群体接触的障碍和促进因素。在大流行前后招募的参与者之间,没有观察到基线特征或结果的差异,尽管对试验的后勤影响是深远的。局限性:该研究没有足够的动力来回答主要的结局问题。COVID-19大流行的发生严重阻碍了目前的试验。结论:该试验不能回答临床和成本效益方面的问题。从该试验中学习可以为新的重新设计的试验提供信息,包括集群随机化,并基于更大、更多样化的人群。未来工作:仍需要对“圆润婴儿”进行明确的试验。最有效的方法可能是进行一项集群随机试验,让主要卫生服务利益相关者和一线从业人员完全接受,以最大限度地招募、参与和参与。试验注册:试验注册号为ISRCTN47575326。资助:该奖项由美国国家卫生与保健研究所(NIHR)公共卫生研究项目(NIHR奖号:15/126/05)资助,全文发表在《公共卫生研究》上;第12卷第17期有关进一步的奖励信息,请参阅美国国立卫生研究院资助和奖励网站。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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