Study protocol for a randomized controlled trial of the effectiveness providing information on childbirth and postnatal period to partners of pregnant wome
Not Applicable
- Conditions
- Paternal depression
- Registration Number
- JPRN-UMIN000021475
- Lead Sponsor
- ational Center for Child Health and Development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 577
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Women who underwent their first prenatal health checkup later than 28 weeks gestation (2) One or both members of the couple is unable to read or write Japanese (3) Individuals undergoing special medical treatment or care for existing mental health problems or poor health due to serious obstetric complications (4) those judged by an investigator to be unsuitable to participate in the study for any other reason.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method