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Clinical Trials/NL-OMON39770
NL-OMON39770
Completed
Not Applicable

The (cost) effectiveness of an online intervention (MamaKits) for pregnant women with affective symptoms: a randomised controlled trial - Mamakits-online study

Vrije Universiteit Medisch Centrum0 sites286 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
angststoornissen en -afwijkingen NEG
Sponsor
Vrije Universiteit Medisch Centrum
Enrollment
286
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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