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The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial
BACKGROUND: Women in pregnancy and postpartum have an increased vulnerability to develop an affective disorder. Affective disorders in pregnancy are associated with an increased risk of prematurity, dysmaturity (foetal weight below the 10(th) percentile as determined by ultrasound) and the developme...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141113/ https://www.ncbi.nlm.nih.gov/pubmed/25123230 http://dx.doi.org/10.1186/1471-2393-14-273 |
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author | Heller, Hanna M van Straten, Annemieke de Groot, Christianne JM Honig, Adriaan |
author_facet | Heller, Hanna M van Straten, Annemieke de Groot, Christianne JM Honig, Adriaan |
author_sort | Heller, Hanna M |
collection | PubMed |
description | BACKGROUND: Women in pregnancy and postpartum have an increased vulnerability to develop an affective disorder. Affective disorders in pregnancy are associated with an increased risk of prematurity, dysmaturity (foetal weight below the 10(th) percentile as determined by ultrasound) and the development of postpartum depressive disorder. Untreated affective disorders and their complications may also result in considerable costs. Recent meta-analyses showed that interventions during pregnancy are less effective than postpartum interventions probably because of high attrition due to the barriers pregnant women experience with attending sessions outside their homes. An internet-based self-help intervention may overcome these barriers as it can be followed at home, and also in one’s own time. Such internet interventions showed to be effective for decreasing affective symptoms in general. This randomised clinical trial examines whether an internet-based self-help intervention is effective in the reduction of affective symptoms in pregnancy and postpartum and results in an improvement of the perinatal outcome. We will also determine the cost-effectiveness of the intervention. METHODS/DESIGN: We will investigate the effectiveness of a 6 week internet-based self-help problem solving treatment (PST) for affective symptoms in pregnancy. We aim to include 286 women with mild to severe affective symptoms who will be randomly assigned to the internet-based intervention or a waiting list control group. Primary outcome measures are affective symptoms and the perinatal outcome. Secondary outcome measures are quality of life, and economic costs. All assessments are based on self-report and will take place at baseline (T0), 10 weeks later (after completion of the intervention (T1), 4 weeks before the expected day of birth (T2), and 6 weeks after delivery (T3). The control group will be measured at the same moments in time. Analysis will be based on the intention-to-treat principle. DISCUSSION: If shown (cost) effective, internet-based PST will offer new possibilities to treat pregnant women for affective symptoms, to improve their perinatal outcome and to prevent the development of postpartum depressive disorders. TRIAL REGISTRATION: Nederlands Trial Register: NTR4321 |
format | Online Article Text |
id | pubmed-4141113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41411132014-08-23 The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial Heller, Hanna M van Straten, Annemieke de Groot, Christianne JM Honig, Adriaan BMC Pregnancy Childbirth Study Protocol BACKGROUND: Women in pregnancy and postpartum have an increased vulnerability to develop an affective disorder. Affective disorders in pregnancy are associated with an increased risk of prematurity, dysmaturity (foetal weight below the 10(th) percentile as determined by ultrasound) and the development of postpartum depressive disorder. Untreated affective disorders and their complications may also result in considerable costs. Recent meta-analyses showed that interventions during pregnancy are less effective than postpartum interventions probably because of high attrition due to the barriers pregnant women experience with attending sessions outside their homes. An internet-based self-help intervention may overcome these barriers as it can be followed at home, and also in one’s own time. Such internet interventions showed to be effective for decreasing affective symptoms in general. This randomised clinical trial examines whether an internet-based self-help intervention is effective in the reduction of affective symptoms in pregnancy and postpartum and results in an improvement of the perinatal outcome. We will also determine the cost-effectiveness of the intervention. METHODS/DESIGN: We will investigate the effectiveness of a 6 week internet-based self-help problem solving treatment (PST) for affective symptoms in pregnancy. We aim to include 286 women with mild to severe affective symptoms who will be randomly assigned to the internet-based intervention or a waiting list control group. Primary outcome measures are affective symptoms and the perinatal outcome. Secondary outcome measures are quality of life, and economic costs. All assessments are based on self-report and will take place at baseline (T0), 10 weeks later (after completion of the intervention (T1), 4 weeks before the expected day of birth (T2), and 6 weeks after delivery (T3). The control group will be measured at the same moments in time. Analysis will be based on the intention-to-treat principle. DISCUSSION: If shown (cost) effective, internet-based PST will offer new possibilities to treat pregnant women for affective symptoms, to improve their perinatal outcome and to prevent the development of postpartum depressive disorders. TRIAL REGISTRATION: Nederlands Trial Register: NTR4321 BioMed Central 2014-08-14 /pmc/articles/PMC4141113/ /pubmed/25123230 http://dx.doi.org/10.1186/1471-2393-14-273 Text en © Heller et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Heller, Hanna M van Straten, Annemieke de Groot, Christianne JM Honig, Adriaan The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
title | The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
title_full | The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
title_fullStr | The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
title_full_unstemmed | The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
title_short | The (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
title_sort | (cost) effectiveness of an online intervention for pregnant women with affective symptoms: protocol of a randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141113/ https://www.ncbi.nlm.nih.gov/pubmed/25123230 http://dx.doi.org/10.1186/1471-2393-14-273 |
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