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Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care
BACKGROUND: To test whether receiving care from a health visitor (HV) trained in identification and psychological intervention methods prevents depression 6–18 months postnatally in women who are not depressed 6 weeks postnatally. METHOD: The study was a prospective cluster trial, randomized by GP p...
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Formato: | Texto |
Lenguaje: | English |
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Cambridge University Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042795/ https://www.ncbi.nlm.nih.gov/pubmed/20716383 http://dx.doi.org/10.1017/S0033291710001467 |
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author | Brugha, T. S. Morrell, C. J. Slade, P. Walters, S. J. |
author_facet | Brugha, T. S. Morrell, C. J. Slade, P. Walters, S. J. |
author_sort | Brugha, T. S. |
collection | PubMed |
description | BACKGROUND: To test whether receiving care from a health visitor (HV) trained in identification and psychological intervention methods prevents depression 6–18 months postnatally in women who are not depressed 6 weeks postnatally. METHOD: The study was a prospective cluster trial, randomized by GP practice, with follow-up for 18 months in 101 primary care teams in the Trent area of England. The participants were women scoring <12 on the postal Edinburgh Postnatal Depression Scale (EPDS) at 6 weeks postnatally (1474 intervention and 767 control women). Intervention HVs (n=89, 63 clusters) were trained in identifying depressive symptoms using the EPDS and face-to-face clinical assessment and in providing psychologically orientated sessions based on cognitive behavioral or person-centered principles. The control group comprised HVs (n=49, 37 clusters) providing care as usual (CAU). The primary outcome measure was the proportion of women scoring ⩾12 on the EPDS at 6 months postnatally. Secondary outcomes were mean EPDS score, Clinical Outcomes in Routine Evaluation – Outcome Measure (CORE-OM) score, State–Trait Anxiety Inventory (STAI), 12-item Short Form Health Survey (SF-12) and Parenting Stress Index Short Form (PSI-SF) scores at 6, 12 and 18 months. RESULTS: After adjusting for individual-level covariates, living alone, previous postnatal depression (PND), the presence of one or more adverse life events and the 6-week EPDS score, the odds ratio (OR) for EPDS ⩾12 at 6 months was 0.71 [95% confidence interval (CI) 0.53–0.97, p=0.031] for the intervention group (IG) women compared with the control (CAU) group women. Two subgroups were formed by baseline severity: a ‘subthreshold’ subgroup with a 6-week EPDS score of 6–11 (n=999) and a ‘lowest severity’ subgroup with a 6-week EPDS score of 0–5 (n=1242). There was no difference in psychological effectiveness by subgroup (interaction term: z=−0.28, p=0.782). CONCLUSIONS: This study provides new evidence of a universal, enduring preventive effect for depression in women who screen negative for depression postnatally. |
format | Text |
id | pubmed-3042795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30427952011-03-23 Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care Brugha, T. S. Morrell, C. J. Slade, P. Walters, S. J. Psychol Med Original Articles BACKGROUND: To test whether receiving care from a health visitor (HV) trained in identification and psychological intervention methods prevents depression 6–18 months postnatally in women who are not depressed 6 weeks postnatally. METHOD: The study was a prospective cluster trial, randomized by GP practice, with follow-up for 18 months in 101 primary care teams in the Trent area of England. The participants were women scoring <12 on the postal Edinburgh Postnatal Depression Scale (EPDS) at 6 weeks postnatally (1474 intervention and 767 control women). Intervention HVs (n=89, 63 clusters) were trained in identifying depressive symptoms using the EPDS and face-to-face clinical assessment and in providing psychologically orientated sessions based on cognitive behavioral or person-centered principles. The control group comprised HVs (n=49, 37 clusters) providing care as usual (CAU). The primary outcome measure was the proportion of women scoring ⩾12 on the EPDS at 6 months postnatally. Secondary outcomes were mean EPDS score, Clinical Outcomes in Routine Evaluation – Outcome Measure (CORE-OM) score, State–Trait Anxiety Inventory (STAI), 12-item Short Form Health Survey (SF-12) and Parenting Stress Index Short Form (PSI-SF) scores at 6, 12 and 18 months. RESULTS: After adjusting for individual-level covariates, living alone, previous postnatal depression (PND), the presence of one or more adverse life events and the 6-week EPDS score, the odds ratio (OR) for EPDS ⩾12 at 6 months was 0.71 [95% confidence interval (CI) 0.53–0.97, p=0.031] for the intervention group (IG) women compared with the control (CAU) group women. Two subgroups were formed by baseline severity: a ‘subthreshold’ subgroup with a 6-week EPDS score of 6–11 (n=999) and a ‘lowest severity’ subgroup with a 6-week EPDS score of 0–5 (n=1242). There was no difference in psychological effectiveness by subgroup (interaction term: z=−0.28, p=0.782). CONCLUSIONS: This study provides new evidence of a universal, enduring preventive effect for depression in women who screen negative for depression postnatally. Cambridge University Press 2011-04 2010-08-18 /pmc/articles/PMC3042795/ /pubmed/20716383 http://dx.doi.org/10.1017/S0033291710001467 Text en Copyright © Cambridge University Press 2010. The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/2.5/>. The written permission of Cambridge University Press must be obtained for commercial re-use. http://creativecommons.org/licenses/by-nc-sa/2.5/ The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/2.5/>. (http://creativecommons.org/licenses/by-nc-sa/2.5/>) The written permission of Cambridge University Press must be obtained for commercial re-use. |
spellingShingle | Original Articles Brugha, T. S. Morrell, C. J. Slade, P. Walters, S. J. Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
title | Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
title_full | Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
title_fullStr | Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
title_full_unstemmed | Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
title_short | Universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
title_sort | universal prevention of depression in women postnatally: cluster randomized trial evidence in primary care |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042795/ https://www.ncbi.nlm.nih.gov/pubmed/20716383 http://dx.doi.org/10.1017/S0033291710001467 |
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