APROPOS-II Study
Recruiting
- Conditions
- Pregnancy, patient tailored care, maternity care, antenatal care, maternal empowerment
- Registration Number
- NL-OMON26863
- Lead Sponsor
- Erasmus Medical Centre - Rotterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 2167
Inclusion Criteria
In order to be eligible to participate in this study, respondents must meet all of the following criteria:
•Above the age of 18 years old
•Pregnant women: presenting at participating midwifery practice for the booking visit
•Prospective father: partner of the participating women.
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study if:
•Less than 18 years of age;
•Inadequate mastery of the Dutch, English, Polish or Turkish language;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of this study will be the improved uptake of PCC and improved lifestyle behaviours
- Secondary Outcome Measures
Name Time Method Secondary outcomes will be the reduction of adverse pregnancy outcomes (e.g. miscarriage, preterm birth, gestational diabetes, etc.) and process evaluation, providing information on the efficacy and feasibility, barriers and facilitators for implementation of the PCC-approach.