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Development and Evaluation of Birth and Parenting Planning Program for Women Who Have Been Diagnosed With Fetal Anomalies

Not Applicable
Conditions
Women who have been diagnosed with fetal anomalies
Registration Number
JPRN-UMIN000033622
Lead Sponsor
St.Luke's International University
Brief Summary

The intervention group had a significantly higher rate submitting BP/BPP (96.0%vs.7.1%, p<0.001) and significantly higher SRESP (t=3.210, p=0.003). The intervention group tended to have higher but non-significant Satisfaction of Care scores. The J-SSQ had no significant differences between the two groups. Women's preferences were both similar and unique. The intervention group had more positive statements (BP/BPP) about their experience.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
61
Inclusion Criteria

Not provided

Exclusion Criteria

Women who have taken psychiatry or psychosomatic medicine. Women who have been diagnosed with Intrauterine fetal death at fist time visiting to research facility. Women who require hospital care in pregnancy by pregnancy complication before onset. Women who are considered in appropriate to participate by obstetrician.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The ratio of women who submit a written preference paper called BP/BPP
Secondary Outcome Measures
NameTimeMethod
Quality data on the description of BP/BPP and questionnaire
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