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不列颠哥伦比亚省产后抑郁和焦虑女性网络心理教育资源的有效性。

Effectiveness of a web-enabled psychoeducational resource for postpartum depression and anxiety among women in British Columbia.

机构信息

Women's Health Research Institute, BC Women's Hospital + Health Centre, Vancouver, BC, Canada.

Department of Obstetrics & Gynaecology, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.

出版信息

Arch Womens Ment Health. 2024 Dec;27(6):995-1010. doi: 10.1007/s00737-024-01468-8. Epub 2024 May 6.

Abstract

PURPOSE

Postpartum depression (PPD) and anxiety (PPA) affect nearly one-quarter (23%) of women in Canada. eHealth is a promising solution for increasing access to postpartum mental healthcare. However, a user-centered approach is not routinely taken in the development of web-enabled resources, leaving postpartum women out of critical decision-making processes. This study aimed to evaluate the effectiveness, usability, and user satisfaction of PostpartumCare.ca, a web-enabled psychoeducational resource for PPD and PPA, created in partnership with postpartum women in British Columbia.

METHODS

Participants were randomized to either an intervention group (n = 52) receiving access to PostpartumCare.ca for four weeks, or to a waitlist control group (n = 51). Measures evaluating PPD (Edinburgh Postnatal Depression Scale) and PPA symptoms (Perinatal Anxiety Screening Scale) were completed at baseline, after four weeks, and after a two-week follow-up. User ratings of website usability and satisfaction and website metrics were also collected.

RESULTS

PPD and PPA symptoms were significantly reduced for the intervention group only after four weeks, with improvements maintained after a two-week follow-up, corresponding with small-to-medium effect sizes (PPD: partial η = 0.03; PPA: partial η = 0.04). Intervention participants were also more likely than waitlist controls to recover from clinical levels of PPD symptoms (χ (1, n = 63) = 4.58, p = .032) and PostpartumCare.ca's usability and satisfaction were rated favourably overall.

CONCLUSION

Findings suggest that a web-enabled psychoeducational resource, created in collaboration with patient partners, can effectively reduce PPD and PPA symptoms, supporting its potential use as a low-barrier option for postpartum women.

TRIAL REGISTRATION

Protocol for this trial was preregistered on NIH U.S. National Library of Medicine, ClinicalTrials.gov as of May 2022 (ID No. NCT05382884).

摘要

目的

产后抑郁症(PPD)和焦虑症(PPA)在加拿大影响近四分之一(23%)的女性。电子健康是增加产后心理健康护理可及性的一种很有前景的解决方案。然而,在开发启用网络的资源时,并未常规采用以用户为中心的方法,这使得产后女性无法参与关键决策过程。本研究旨在评估 PostpartumCare.ca 的有效性、可用性和用户满意度,这是一个针对 PPD 和 PPA 的启用网络的心理教育资源,是与不列颠哥伦比亚省的产后女性合作创建的。

方法

参与者被随机分配到干预组(n=52),接受 PostpartumCare.ca 的访问权限四周,或等待名单对照组(n=51)。使用评估 PPD(爱丁堡产后抑郁量表)和 PPA 症状(围产期焦虑筛查量表)的措施在基线、四周后和两周随访时完成。还收集了网站可用性和满意度以及网站指标的用户评分。

结果

只有干预组的 PPD 和 PPA 症状在四周后显著降低,并且在两周随访后保持改善,这与小到中等的效应大小相对应(PPD:偏 η=0.03;PPA:偏 η=0.04)。与等待名单对照组相比,干预组参与者也更有可能从 PPD 症状的临床水平中恢复( χ (1, n=63)=4.58, p=0.032),并且总体上对 PostpartumCare.ca 的可用性和满意度评价较高。

结论

研究结果表明,与患者合作伙伴共同创建的启用网络的心理教育资源可以有效减轻 PPD 和 PPA 症状,这支持了其作为产后女性低门槛选择的潜在用途。

试验注册

该试验的方案于 2022 年 5 月在美国国立卫生研究院美国国家医学图书馆、临床试验.gov 上预先注册,编号为 NCT05382884。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9234/11579107/a7fa97125d26/737_2024_1468_Fig1_HTML.jpg

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