CH Annecy Genevois
Épagny, Auvergne-Rhône-Alpes, 74370, France
NCT Number: NCT07653646
Maternal mental health in the postpartum period is a major public health issue in France. The 2021 National Perinatal Survey highlights high prevalence rates of mental health disorders among mothers, with 27.6% experiencing anxiety disorders, 16.7% experiencing depressive disorders and 5.4% having suicidal thoughts. Between 2016 and 2018, suicide was also the leading cause of maternal mortality in the year following childbirth, underscoring the severity and frequency of these disorders. In response, international guidelines, notably those of the World health Organisation (WHO), as well as national policies such as the 'First 1,000 Days' strategy, emphasise the importance of early, enhanced and individualised postnatal support. In France, this postpartum care tends to be structured around the Early Postnatal Interview and the recommended use of validated screening tools such as the Edinburgh Postnatal Depression Scale (EPDS).
However, the quality of postpartum care depends not only on screening and clinical follow-up, but also on organisational and environmental factors. Among these, the arrangements for maternity ward visits constitute a potential determinant of patients' experiences, likely to influence both their mental state, their rest, the establishment of breastfeeding and, indirectly, the health of the newborn. The exceptional measures implemented during the Covid-19 pandemic, notably the restriction of visits, have shown generally favourable effects, with improved satisfaction among patients and healthcare staff, better conditions for rest, facilitation of breastfeeding and a perceived improvement in working conditions.
However, these data were collected in an exceptional health context, which may introduce biases linked to the social, emotional and organisational constraints specific to this period. Their extrapolation to routine practice therefore remains uncertain. Furthermore, in the absence of specific national guidelines governing maternity ward visits, the current regulatory framework remains unclear and practices vary between institutions, often relying on local decisions that have not been scientifically evaluated.
Against this backdrop, the VISIMAT study aims to characterise maternity ward visiting arrangements outside of any exceptional circumstances and to assess their impact on the health of mothers and newborns, as well as on healthcare workers' working conditions. Its aim is to provide a scientific basis to inform the development of standardised recommendations and prevention messages.
Trial opening soon.
Get Notified18 year and older
Female
Interventional
Not applicable
Épagny, Auvergne-Rhône-Alpes, 74370, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The only intervention resulting from the research consists of referring patients with an EPDS score ≥ 10 and/or a positive response to item 10 of this scale ('has already thought about harming themselves') to a psychologist.
Time frame: At discharge from hospitalization in the maternity ward, on average 48 hours
The incidence of depressive symptoms in the mother using the Edinburgh Postnatal Depression Scale (EPDS)
Time frame: Until discharge from hospitalization in the maternity ward, on average 48 hours.
Neonatal weight change between birth and discharge from the maternity ward, reflecting the newborn's early health status.
Contact information is provided by the study sponsor or research team.
Centre Hospitalier Annecy Genevois
Other
Restrictions on Maternity Ward Visits: Current Situation, Challenges and Recommendations in the AuRA Region
Acronym: VISIMAT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06845423
Cardiovascular Diseases, Embolism and Thrombosis
Amiens, France
View Trial DetailsNCT07280000
Behavior, Breast Feeding
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT07029282
Adaptive Trial, Multiple Micronutrient Deficiencies During Pregnancy
Karachi, Sindh, Pakistan
View Trial DetailsNCT06865391
18 Years and Over, 37 or More Completed Weeks of Gestation
Kahramanmaraş Merkez, K.maraş, Turkey (Türkiye)
View Trial Details