NL-OMON39770CompletedNot Applicable
The (cost) effectiveness of an online intervention (MamaKits) for pregnant women with affective symptoms: a randomised controlled trial - Mamakits-online study
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 286
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 to 99 (—)
Inclusion Criteria
- •participants are included if:
- •1 they are pregnant in any stage of their pregnancy until 10 weeks before the expected date of delivery
- •2 they are 18 years or older and
- •3 they return an informed consent and
- •4 they have symptoms of depression and/or anxiety as defined by scoring above the cut-off of 15 ( *16) on the in the Center for Epidemiological Studies Depression scale (CES-D) and/or above the cut-off of 7 ( * 8) on the Hospital Anxiety and Depressionscale (HADS) and
- •5 they have access to a computer and
- •6 they have sufficient knowledge of the Dutch language
Exclusion Criteria
- •Exclusion criteria are:
- •1.age under 18
- •2.expected delivery date within 10 weeks. These women will be offered the intervention 6 weeks after giving birth at the same time as the controlgroup.
- •3.Symptoms are to mild as defined by a CES-D <16 and/or a HADS-A < 8
- •4. Severe suicidality as measured with one question of the Screening Questionnaire. Here the cut-off score is 3
Investigators
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