Effectiveness of a web-enabled psychoeducational resource for postpartum depression and anxiety among women in British Columbia.

Autor:	Lawrence, Claire G, Breau, Genevieve, Yang, Lily, Hellerstein, Orli S, Hippman, Catriona, Kennedy, Andrea L, Ryan, Deirdre, Shulman, Barbara, Brotto, Lori A
Předmět:	ANXIETY prevention WOMEN'S education EDINBURGH Postnatal Depression Scale WORLD Wide Web RESEARCH funding INTERPROFESSIONAL relations EDUCATIONAL outcomes STATISTICAL sampling DIGITAL health POSTPARTUM depression PSYCHOEDUCATION RANDOMIZED controlled trials DESCRIPTIVE statistics INFORMATION resources ANXIETY CHI-squared test TELEMEDICINE SURVEYS USER-centered system design PATIENT satisfaction
Zdroj:	Archives of Women's Mental Health; Dec2024, Vol. 27 Issue 6, p995-1010, 16p
Abstrakt:	Purpose: Postpartum depression (PPD) and anxiety (PPA) affect nearly one-quarter (23%) of women in Canada. eHealth is a promising solution for increasing access to postpartum mental healthcare. However, a user-centered approach is not routinely taken in the development of web-enabled resources, leaving postpartum women out of critical decision-making processes. This study aimed to evaluate the effectiveness, usability, and user satisfaction of PostpartumCare.ca, a web-enabled psychoeducational resource for PPD and PPA, created in partnership with postpartum women in British Columbia. Methods: Participants were randomized to either an intervention group (n = 52) receiving access to PostpartumCare.ca for four weeks, or to a waitlist control group (n = 51). Measures evaluating PPD (Edinburgh Postnatal Depression Scale) and PPA symptoms (Perinatal Anxiety Screening Scale) were completed at baseline, after four weeks, and after a two-week follow-up. User ratings of website usability and satisfaction and website metrics were also collected. Results: PPD and PPA symptoms were significantly reduced for the intervention group only after four weeks, with improvements maintained after a two-week follow-up, corresponding with small-to-medium effect sizes (PPD: partial η2 = 0.03; PPA: partial η2 = 0.04). Intervention participants were also more likely than waitlist controls to recover from clinical levels of PPD symptoms (χ 2 (1, n = 63) = 4.58, p =.032) and PostpartumCare.ca's usability and satisfaction were rated favourably overall. Conclusion: Findings suggest that a web-enabled psychoeducational resource, created in collaboration with patient partners, can effectively reduce PPD and PPA symptoms, supporting its potential use as a low-barrier option for postpartum women. Trial Registration: Protocol for this trial was preregistered on NIH U.S. National Library of Medicine, ClinicalTrials.gov as of May 2022 (ID No. NCT05382884). [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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