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Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial
OBJECTIVE: Perinatal depression (PND) is a severe complication of pregnancy, affecting both mothers and newborns. Bright light therapy (BLT) has only been tested in a few studies for treating either antenatal or postnatal depression. We conducted a pilot trial to investigate the efficacy and safety...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804451/ https://www.ncbi.nlm.nih.gov/pubmed/35876837 http://dx.doi.org/10.1111/acps.13482 |
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author | Garbazza, Corrado Cirignotta, Fabio D'Agostino, Armando Cicolin, Alessandro Hackethal, Sandra Wirz‐Justice, Anna Cajochen, Christian Manconi, Mauro |
author_facet | Garbazza, Corrado Cirignotta, Fabio D'Agostino, Armando Cicolin, Alessandro Hackethal, Sandra Wirz‐Justice, Anna Cajochen, Christian Manconi, Mauro |
author_sort | Garbazza, Corrado |
collection | PubMed |
description | OBJECTIVE: Perinatal depression (PND) is a severe complication of pregnancy, affecting both mothers and newborns. Bright light therapy (BLT) has only been tested in a few studies for treating either antenatal or postnatal depression. We conducted a pilot trial to investigate the efficacy and safety of BLT for PND occurring at any time across the perinatal period. METHODS: A single‐blind RCT was carried out in women with an EPDS >12 from the 2nd gestational trimester until 9 months postpartum. Participants received either 30‐minutes morning BLT (10′000 lux) or dim red light (DRL, 19 lux) for 6 weeks. RESULTS: Twenty‐two women were randomised to BLT (n = 11) or DRL (n = 11). Among those receiving BLT, 73% achieved remission (improvement ≥50%, EPDS score ≤ 12), in contrast to 27% in the DRL group (p = 0.04). A significant influence of time on EPDS score and group‐time interaction emerged, with a greater reduction in the BLT‐group across the follow‐up period. No women in either group reported major side effects. CONCLUSION: Morning BLT induced a significant remission from PND as compared to DRL and this effect was maintained across the perinatal period. BLT showed an excellent safety profile and was well‐tolerated, thus representing a valid therapeutic strategy in this vulnerable perinatal population. |
format | Online Article Text |
id | pubmed-9804451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98044512023-01-03 Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial Garbazza, Corrado Cirignotta, Fabio D'Agostino, Armando Cicolin, Alessandro Hackethal, Sandra Wirz‐Justice, Anna Cajochen, Christian Manconi, Mauro Acta Psychiatr Scand Original Articles OBJECTIVE: Perinatal depression (PND) is a severe complication of pregnancy, affecting both mothers and newborns. Bright light therapy (BLT) has only been tested in a few studies for treating either antenatal or postnatal depression. We conducted a pilot trial to investigate the efficacy and safety of BLT for PND occurring at any time across the perinatal period. METHODS: A single‐blind RCT was carried out in women with an EPDS >12 from the 2nd gestational trimester until 9 months postpartum. Participants received either 30‐minutes morning BLT (10′000 lux) or dim red light (DRL, 19 lux) for 6 weeks. RESULTS: Twenty‐two women were randomised to BLT (n = 11) or DRL (n = 11). Among those receiving BLT, 73% achieved remission (improvement ≥50%, EPDS score ≤ 12), in contrast to 27% in the DRL group (p = 0.04). A significant influence of time on EPDS score and group‐time interaction emerged, with a greater reduction in the BLT‐group across the follow‐up period. No women in either group reported major side effects. CONCLUSION: Morning BLT induced a significant remission from PND as compared to DRL and this effect was maintained across the perinatal period. BLT showed an excellent safety profile and was well‐tolerated, thus representing a valid therapeutic strategy in this vulnerable perinatal population. John Wiley and Sons Inc. 2022-08-03 2022-10 /pmc/articles/PMC9804451/ /pubmed/35876837 http://dx.doi.org/10.1111/acps.13482 Text en © 2022 The Authors. Acta Psychiatrica Scandinavica published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Garbazza, Corrado Cirignotta, Fabio D'Agostino, Armando Cicolin, Alessandro Hackethal, Sandra Wirz‐Justice, Anna Cajochen, Christian Manconi, Mauro Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial |
title | Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial |
title_full | Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial |
title_fullStr | Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial |
title_full_unstemmed | Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial |
title_short | Sustained remission from perinatal depression after bright light therapy: A pilot randomised, placebo‐controlled trial |
title_sort | sustained remission from perinatal depression after bright light therapy: a pilot randomised, placebo‐controlled trial |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804451/ https://www.ncbi.nlm.nih.gov/pubmed/35876837 http://dx.doi.org/10.1111/acps.13482 |
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