Ugarte Amaia Ugarte, López-Peña Purificación, Vangeneberg Carmen Serrulla, Royo Julia Gemma Torregaray, Ugarte Maria Asunción Arrieta, Compains Maria Teresa Zabalza, Medrano Maria Pilar Riaño, Toyos Nerea Muñoz, Lamo Edurne Arenaza, Dueñas Maria Begoña Beneitez, González-Pinto Ana
Department of Psychiatry, University Hospital of Alava-Santiago, Vitoria, Spain.
Centre for Biomedical Research Network on Mental Health (CIBERSAM), Madrid, Spain.
BMC Psychiatry. 2017 Jan 13;17(1):13. doi: 10.1186/s12888-016-1162-5.
Postpartum depression is a disease with a prevalence of 20% that has deleterious consequences not only for the mother but also for the baby and can cause delays in physical, social and cognitive development. In this context, the European Union Committee on Public Health has declared it essential that preventative measures are taken by centres providing care for women with a multidisciplinary approach. PROGEA is a multicentre, single-blind randomized, 3-year, longitudinal clinical trial aiming to evaluate the efficacy of a psychoeducational programme in preventing postpartum depression in at-risk women, based on a range of clinical variables, and explore prognostic factors. This paper describes the methods and rationale behind the study.
We will study women receiving treatment as usual plus a psychoeducation cognitive behavioural therapy (CBT)-based intervention and a control group receiving only treatment as usual. The sample will be recruited from an incidental sampling of pregnant women in two health regions. We will recruit 600 women in the third trimester of pregnancy who consent to take part in the study. Almost half of the women, about 280, would be expected to have some risk factors for postpartum depression. All those found to have risk factors will be evaluated, and we estimate that a quarter will be classified as at-risk of developing postpartum depression as measured with the Edinburgh Postnatal Depression Scale. This subset will be randomly allocated to receive treatment as usual with or without the CBT intervention. Six sessions of CBT (1 individual and 5 group) will be offered by a psychologist.
Findings from this study will be used to design a definitive study that will examine the clinical and cost-effectiveness of the CBT-based intervention in improving the mood of women in the postpartum period.
ClinicalTrials.gov Identifier: NCT02323152 ; Date: December 2014.
产后抑郁症是一种患病率达20%的疾病,不仅对母亲有有害影响,对婴儿也有影响,且会导致身体、社交和认知发展方面的延迟。在此背景下,欧盟公共卫生委员会宣称,为女性提供护理的中心采取多学科方法的预防措施至关重要。PROGEA是一项多中心、单盲随机、为期3年的纵向临床试验,旨在基于一系列临床变量评估心理教育项目对预防高危女性产后抑郁症的疗效,并探索预后因素。本文描述了该研究背后的方法和基本原理。
我们将研究接受常规治疗加基于认知行为疗法(CBT)的心理教育干预的女性,以及仅接受常规治疗的对照组。样本将从两个健康地区的孕妇偶然抽样中招募。我们将招募600名妊娠晚期同意参与研究的女性。预计几乎一半的女性,约280人,会有一些产后抑郁症的风险因素。所有被发现有风险因素的女性都将接受评估,我们估计四分之一的女性会被归类为有患产后抑郁症的风险,这是根据爱丁堡产后抑郁量表测量得出的。这个子集将被随机分配接受有或没有CBT干预的常规治疗。一名心理学家将提供六次CBT治疗(1次个体治疗和5次团体治疗)。
本研究的结果将用于设计一项确定性研究,该研究将检验基于CBT的干预在改善产后女性情绪方面的临床效果和成本效益。
ClinicalTrials.gov标识符:NCT02323152;日期:2014年12月。