Título Effectiveness of psychological, psychoeducational and psychosocial interventions to prevent postpartum depression in adolescent and adult mothers: study protocol for a systematic review and meta-analysis of randomised controlled trials.
Autores MARTÍN GÓMEZ, CARMEN, Moreno-Peral, Patricia , Bellon, Juan A , Conejo Ceron, Sonia , Campos-Paino, Henar , GÓMEZ GÓMEZ, IRENE, RIGABERT SÁNCHEZ-JUNCO, ALINA, BENÍTEZ BAENA, ISABEL, MOTRICO MARTINEZ, EMMA
Publicación externa No
Medio BMJ Open
Alcance Article
Naturaleza Científica
Cuartil JCR 2
Cuartil SJR 1
Impacto JCR 2.69200
Impacto SJR 1.13200
Web https://www.scopus.com/inward/record.uri?eid=2-s2.0-85084785405&doi=10.1136%2fbmjopen-2019-034424&partnerID=40&md5=9c4e550e8a9926418598779a3e6679ef
Fecha de publicacion 17/05/2020
ISI 000738373200041
Scopus Id 2-s2.0-85084785405
DOI 10.1136/bmjopen-2019-034424
Abstract INTRODUCTION: The prevalence of postpartum depression (PPD) is 17%, and\n the incidence is 12% worldwide. Adverse consequences for mothers and\n babies have been associated with this disease. To assess the\n effectiveness of psychological, psychoeducational and psychosocial\n interventions in preventing PPD, a systematic review and meta-analysis\n (SR/MA) will be conducted.\n METHODS AND ANALYSIS: A SR/MA will be performed following the\n indications of the Preferred Reporting Items for Systematic Reviews and\n Meta-Analyses guidelines. Studies will be identified through MEDLINE\n (Ovid and PubMed), PsycINFO, Web of Science, Scopus, CINAHL, Cochrane\n Central Register of Controlled Trials, OpenGrey, Australian New Zealand\n Clinical Trial Registry, ClinicalTrials.gov and evidencebasedtherapy.org\n from inception until 31 January 2020. Bridging searches will be also\n conducted until the review is completed. The selection criteria will be\n as follows: (1) subjects will be pregnant females or females who have\n given birth in the last 12 months and who were non-depressive at\n baseline; (2) psychological, psychoeducational and psychosocial\n interventions; (3) comparator will be usual care, attention control,\n waiting list or no intervention; (4) outcomes will be specific results\n on PPD; and (5) the design of the studies will be randomised controlled\n trials. No restrictions regarding the year of publication, the setting\n of the intervention or the language of publication will be considered.\n Pooled standardised mean differences and 95% CIs will be calculated. The\n risk of bias of the studies will be assessed through the Cochrane\n Collaboration risk of bias tool. Heterogeneity between the studies will\n be determined by the I2 and Cochran\'s Q statistics. Sensitivity and\n subgroup analyses will also be performed. Publication bias will be\n checked with funnel plots and Egger\'s test. Heterogeneity will be\n explored by random-effects meta-regression analysis.\n ETHICS AND DISSEMINATION: The ethical assessment was not required. The\n results will be presented at conferences and disseminated through\n publications.\n PROSPERO REGISTRATION NUMBER: CRD42018109981.
Palabras clave adolescent; adult; cognitive behavioral therapy; follow up; human; interpersonal psychotherapy; meta analysis (topic); postnatal depression; psychoeducation; psychotherapy; Review; social environment;
Miembros de la Universidad Loyola

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