High-risk Pregnant Women Diagnosed with Threatened Premature Labor, Cervical Incompetency, Premature Rupture of the Membranes, Placenta Previa, Hypertensive Disorders of Pregnancy and Fetal Growth Restriction
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: This study includes only singleton pregnancies. Upon admission, the pregnant woman must be between 24 and 35 weeks' gestation. Additionally, fetal well-being has been confirmed.Symptoms have been stabilized with post-hospitalization treatment and the pregnancy is expected to continue for at least one week after admission.
Exclusion criteria
Exclusion criteria: Pregnant women with psychiatric complications, multiple gestations, fetal diseases, or who are unable to communicate in Japanese.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The change in STAI (State-Trait Anxiety Inventory) scores before and after the program intervention is calculated for each case. | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in the EPDS (Edinburgh Postnatal Depression Scale), PHQ-9 (Patient Health Questionnaire-9), GAD-7 (Generalized Anxiety Disorder-7), MIBS-J (Mother to Infant Bonding Scale-Japanese version) and EQ-5D-5L (EuroQol-5dimension-5level) before and after the program. Post-program impressions. | — |
Countries
Japan
Contacts
Tokyo Women's Medical University Yachiyo Medical Center Nursing Department