The effectiveness of een internet course for pregnant women with depressive and anxiety symptoms
- Conditions
- pregnancy, affective symptoms, depressive symptoms, anxiety symptoms, depression, anxiety, online interventions, low birth weight, prematurity and breastfeeding, zwangerschap, depressie, angst, prematuriteit, borstvoeding, internet interventie.
- Registration Number
- NL-OMON20793
- Lead Sponsor
- VU medical center
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 286
Inclusion Criteria
participants of 18 years and older,
who are pregnant at any stage of pregnancy, but not later than 10 weeks before the expected delivery date,
Who have at least mild symptoms of depression and/or anxiety, defined by Center for Epidemiological Studies Depression scale (CES-D) higher than 16 and /or a score higher than 8 on the Hospital Anxiety and Depression scale (HADS-A)
Exclusion Criteria
Participants who indicate that they either intend to harm themselves or to attempt suicide (as assessed by one question [210]) will be excluded and advised to consult their general practitioner to obtain more tailored care.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. reduction of depressive and anxiety symptoms post intervention and 6 weeks postpartum <br /><br>2 improvement in perinatal outcome (e.g.pre-term birth, growth restriction and breastfeeding initiation)<br />
- Secondary Outcome Measures
Name Time Method 1. Cost effectiveness of the intervention<br /><br>2. Quality of life<br />