Postpartum DepressionNCT01423331
An Evaluation and Factor Analysis for Maternal Mental Health
An observational study of Postpartum Depression, run by Shin Kong Wu Ho-Su Memorial Hospital.
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. Read more about this study
- Who is it for?
- Ages 20 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Postpartum Depression
- How many people
- 200 participants
- Where
- No sites listed yet
- Study dates
- Aug 2011to Dec 2012
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 years and older
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Study population: the pregnant women or mothers within six months after birth
Who may be able to join
- the pregnant women or mothers within six months after birth
Who cannot join
- Minor
Trial locations and contacts
No sites are listed yet.
About this study
Official title: An Evaluation and Factor Analysis for Maternal Mental Health - The Analytic Study of the Shin Kong Wu Ho-Su Memorial Hospital
An Evaluation and Factor Analysis for Maternal Mental Health - The Analytic Study of the Shin Kong Wu Ho-Su Memorial Hospital
- Objectives：
- To construct a screening tool for domestic maternal mental health
- To expect to find the screening timing for early assessment or intervention of domestic maternal mental health status.
- To explore the impact of domestic maternal mental health factors.
Read the detailed 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：
- Expected to construct the applicable domestic early assessment screening or intervention time of maternal mental health status.
- Expected to develop different screening tools for a domestic early assessment of the maternal mental health status.
- Expected to identify the important factors of maternal depression to provide a reference for locking in a high risk group for early intervention.
- The implementation of women's health policy on mental health care of pregnant women with specific feasible approach.
- 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.
- Conditions
- Postpartum Depression
- Keywords
- Postpartum depression, maternal mental health
- Medical subject headings
- Depression, Postpartum
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Aug 2011 (estimated)
- Study startAug 2011
- Primary completionDec 2012 (estimated)
- Study completionDec 2012 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Postpartum DepressionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Shin Kong Wu Ho-Su Memorial Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Department of Health, Executive Yuan, R.O.C. (Taiwan)
- Responsible party
- Principal investigator, Yieh-Loong Tsai, Shin Kong Wu Ho-Su Memorial Hospital
- Investigators
- Yieh-Loong Tsai, Study chair, Shin Kong Wu Ho-Su Memorial Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01423331
- Sponsor's protocol ID
- 20110409R
- Status last verified
- Aug 2011
- First submitted
- 24 Aug 2011
- Last updated
- 25 Aug 2011
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 25 Aug 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- An Evaluation and Factor Analysis for Maternal Mental Health - The Analytic Study of the Shin Kong Wu Ho-Su Memorial Hospital
- ClinicalTrials.gov ID
- NCT01423331
- Acronym / sponsor ID
- 20110409R
- Conditions
- Postpartum Depression
- Keywords
- Postpartum depression, maternal mental health
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Shin Kong Wu Ho-Su Memorial HospitalUniversity, hospital or other
- Collaborators
- Department of Health, Executive Yuan, R.O.C. (Taiwan)
- Study start
- Aug 2011
- Primary completion
- Dec 2012 (estimated)
- Study completion
- Dec 2012 (estimated)
- First posted
- 25 Aug 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
An Evaluation and Factor Analysis for Maternal Mental Health - The Analytic Study of the Shin Kong Wu Ho-Su Memorial Hospital
- Objectives：
- To construct a screening tool for domestic maternal mental health
- To expect to find the screening timing for early assessment or intervention of domestic maternal mental health status.
- To explore the impact of domestic maternal mental health factors.
Detailed 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：
- Expected to construct the applicable domestic early assessment screening or intervention time of maternal mental health status.
- Expected to develop different screening tools for a domestic early assessment of the maternal mental health status.
- Expected to identify the important factors of maternal depression to provide a reference for locking in a high risk group for early intervention.
- The implementation of women's health policy on mental health care of pregnant women with specific feasible approach.
- 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
Who may qualify
- Ages
- 20 years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- the pregnant women or mothers within six months after birth
Key inclusion criteria (1 listed)
- the pregnant women or mothers within six months after birth
Key exclusion criteria (1 listed)
- Minor
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Aug 2011.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Yieh-Loong Tsai study chair
Shin Kong Wu Ho-Su Memorial Hospital
Questions about this trial
What is this clinical trial studying?
An observational study of Postpartum Depression, run by Shin Kong Wu Ho-Su Memorial Hospital.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 25 Aug 2011. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Yieh-Loong Tsai (+886-968995265, m002044@ms.skh.org.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Aug 2011.