An Evaluation & Factor Analysis for Maternal Mental Health

Status Not yet recruiting

Clinical Trial Summary

An Evaluation and Factor Analysis for Maternal Mental Health - The Analytic Study of the Shin Kong Wu Ho-Su Memorial Hospital

- Objectives：

1. To construct a screening tool for domestic maternal mental health

2. To expect to find the screening timing for early assessment or intervention of domestic maternal mental health status.

3. To explore the impact of domestic maternal mental health factors.

Clinical Trial Description

-Study Design： This project will be conducted at the Shin Kong Memorial Hospital for pregnant women or mothers within six months after birth, with the base of existing domestic and foreign screening tools for postpartum depression and the related scale modeled, and select respective women during different pregnant period and after birth as postpartum study, by longitudinal study and cross-sectional study of the advantages to be able to plan time for up to twelve months of data collection, able to undertake within-subjects comparison and the between-subjects comparison, to view depression during pregnancy , pregnancy depression, postpartum blues, postpartum depression, postpartum psychosis such as prevalence, risk factors or any other factors.

To establish the screening tool and screening time for national early assessment of maternal mental health status of women in pregnancy and after birth.

-Effect：

1. Expected to construct the applicable domestic early assessment screening or intervention time of maternal mental health status.

2. Expected to develop different screening tools for a domestic early assessment of the maternal mental health status.

3. Expected to identify the important factors of maternal depression to provide a reference for locking in a high risk group for early intervention.

4. The implementation of women's health policy on mental health care of pregnant women with specific feasible approach.

5. To provide mental health counseling, the implementation of the operation of the network of community resources to reduce maternal stress in coping to new life. ;

Study Design

N/A

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01423331
Study type	Observational
Source	Shin Kong Wu Ho-Su Memorial Hospital
Contact	Yieh-Loong Tsai
Phone	+886-968995265
Email	m002044@ms.skh.org.tw
Status	Not yet recruiting
Phase	N/A
Start date	August 2011
Completion date	December 2012

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.