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Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA
BACKGROUND: 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 e...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237273/ https://www.ncbi.nlm.nih.gov/pubmed/28086766 http://dx.doi.org/10.1186/s12888-016-1162-5 |
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author | 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 |
author_facet | 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 |
author_sort | Ugarte, Amaia Ugarte |
collection | PubMed |
description | BACKGROUND: 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. METHODS: 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. DISCUSSION: 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. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02323152; Date: December 2014. |
format | Online Article Text |
id | pubmed-5237273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52372732017-01-18 Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA 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 BMC Psychiatry Study Protocol BACKGROUND: 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. METHODS: 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. DISCUSSION: 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. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02323152; Date: December 2014. BioMed Central 2017-01-13 /pmc/articles/PMC5237273/ /pubmed/28086766 http://dx.doi.org/10.1186/s12888-016-1162-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol 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 Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA |
title | Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA |
title_full | Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA |
title_fullStr | Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA |
title_full_unstemmed | Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA |
title_short | Psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, PROGEA |
title_sort | psychoeducational preventive treatment for women at risk of postpartum depression: study protocol for a randomized controlled trial, progea |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237273/ https://www.ncbi.nlm.nih.gov/pubmed/28086766 http://dx.doi.org/10.1186/s12888-016-1162-5 |
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