| Title: |
Study protocol for improving mental health during pregnancy: a randomized controlled low-intensity m-health intervention by midwives at primary care centers. |
| Authors: |
Jimenez-Barragan, Marta1,2,3 (AUTHOR) marta.jim@gmail.com, del Pino Gutierrez, Amparo4,5 (AUTHOR), Garcia, Jorge Curto4 (AUTHOR), Monistrol-Ruano, Olga6 (AUTHOR), Coll-Navarro, Engracia7 (AUTHOR), Porta-Roda, Oriol8 (AUTHOR), Falguera-Puig, Gemma2,9 (AUTHOR) |
| Source: |
BMC Nursing. 9/7/2023, Vol. 22 Issue 1, p1-9. 9p. 1 Color Photograph, 1 Diagram. |
| Subject Terms: |
*MENTAL health, *RANDOMIZED controlled trials, *LONGITUDINAL method, *HEALTH facilities |
| Abstract: |
Background: Pregnancy-related anxiety and depression has received considerable attention worldwide. Mental health problems in pregnant women already since early weeks of gestation may have important consequences to the fetus. The necessity for more effective health care pathways, including some early interventions that reduce the overall burden of the childbearing situation appears a key factor for a successful birth and care of the baby. The few studies focalized in interventions, are focused on delivery and postpartum, without taking into account the whole maternity process. Current literature recommends the use of interventions based on new technologies for the treatment of mood disorders, already during the prenatal period. There have been scarce well-designed intervention studies that test technological low-intensity interventions by midwives to address pregnant women's mental health, diminishing anxiety and depression during pregnancy. Methods/design: Adult pregnant women (weeks 12–14 of gestation) will be recruited and screened from different primary care centers in Catalonia, Spain. Women who pass the initial mental screening will be randomly allocated to the relaxation virtual reality intervention or control group. The intervention aims to improve mental state of pregnant women during pregnancy, work through breathing, mindfulness and muscle relaxation techniques. Women in the control group will receive standard care offered by the public funded maternity services in Catalonia. The primary outcome measures will include the Edinburg Postnatal Depression (EPDS), State Trait Anxiety Inventory (STAI), Symptom Checklist-90 (SCL-90), and the Cambridge Worry Scale (CWS) instruments. Secondary outcome measures will include the Temperament and Character Inventory-Revised (TCI-R) and the Whooley and Generalized Anxiety Disorder-2 (GAD-2) questions. Routinary pregnancy monitoring measures will be also evaluated. Discussion: This study aims to test the efficacy of a low-intensity, midwife-led e-health intervention based on new technologies to work on women's anxiety and depression during pregnancy. We hypothesize that low-intensity mental health intervention during pregnancy, using an e-health (virtual reality) as a support tool, will be effective in reducing of anxiety, depressive symptoms, and improving satisfaction with pregnancy follow-up. Trial registration: Clinical Trials ID NCT05756205. [ABSTRACT FROM AUTHOR] |
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