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Clinical Trials/NCT05830266
NCT05830266
Recruiting
Not Applicable

Mother-infant Bonding in the Brain: Promoting Maternal Mental Health and High-quality Mother-infant Interactions Via a Mindfulness-based Intervention

Tilburg University1 site in 1 country64 target enrollmentJuly 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postpartum Depression
Sponsor
Tilburg University
Enrollment
64
Locations
1
Primary Endpoint
Change from baseline postpartum anxiety symptoms
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

The study investigates the effectiveness of the mindfulness-based intervention "Mindful with your Baby" in women with babies between 5-9 months postpartum who experience heightened levels of postpartum depression, anxiety and/or parental stress. The intervention "Mindful with your Baby" is one of the very few interventions for maternal postnatal mental health issues that takes the bond between mother and infant into account. It is hypothesized that the "Mindful with your Baby" intervention will reduce levels of postpartum depression, anxiety and parental stress, and improve mother-infant behavioral interaction and increase neural synchrony between mother and infant brains.

Registry
clinicaltrials.gov
Start Date
July 1, 2023
End Date
September 1, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Tilburg University
Responsible Party
Principal Investigator
Principal Investigator

Marion van den Heuvel

Principal Investigator

Tilburg University

Eligibility Criteria

Inclusion Criteria

  • Pregnant women (18+y).
  • First antenatal visit \< 12 weeks.
  • Score above cut off on the Edinburgh Postnatal Depression Scale (EPDS), the anxiety subscale of the Symptom Checklist (SCL-90) and/or the Parental Stress Questionnaire (PSQ) at 8-10 weeks postpartum.
  • Dutch-speaking or understanding Dutch.

Exclusion Criteria

  • Gemelli pregnancy (or higher order pregnancy).
  • Known endocrine disorder before pregnancy (diabetes-I, Rheumatoid arthritis).
  • Severe psychiatric disease (schizophrenia, borderline or bipolar disorder).
  • Drug or alcohol addiction problems.
  • Any other disease resulting in treatment with drugs that are potentially adverse for the fetus and need careful follow-up during pregnancy.
  • No access to the internet.

Outcomes

Primary Outcomes

Change from baseline postpartum anxiety symptoms

Time Frame: before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18)

Assessed with the 10-item anxiety subscale of the Symptom Checklist (SCL-90). The total scores range from 10 to 50 and higher scores reflect more anxiety symptoms. The questionnaire has showed good reliability and validity in non-pregnant samples.

Change from baseline mother-infant bonding

Time Frame: Before the intervention (baseline, week 0) and post-intervention (week 8)

Assessed with video coding

Change from baseline neural synchrony between mother and infant (EEG outcome 2)

Time Frame: Before the intervention (baseline, week 0) and post-intervention (week 8)

Assessed with dual-EEG, with the Phase Locking Value (PLV) in the alpha band frequency (6-9 Hz) during the still face paradigm. We expect that neural synchrony between mother and infant will increase (more) in the intervention group.

Change from baseline postpartum depressive symptoms

Time Frame: before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18)

Assessed with the 10-item Edinburgh Postnatal Depression Scale (EPDS). The EPDS is the most widely used self-rating scale to assess depressive symptoms in the perinatal period. The EPDS total score ranges from 0 to 30, with higher scores indicating more depressive symptoms. The questionnaire has been validated in Dutch postpartum women.

Change from baseline parental stress

Time Frame: before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18)

Assessed with the Parental Stress Questionnaire (PSQ, in Dutch: Opvoedingsbelastingvragenlijst), which is based on the Parenting Stress Index. This study uses only the first three subscales related to parenting: parent-child relationship problems, parenting problems and parental role restriction. Total scores range from 19 to 76 with higher scores indicating more parental stress. In order to interpret the level of parental stress experienced, subscale scores are converted into T-scores conform the norms of the child's age (e.g., 0 to 3 years). The questionnaire and subscales have showed good reliability and validity.

Change from baseline neural synchrony between mother and infant (EEG outcome 1)

Time Frame: Before the intervention (baseline, week 0) and post-intervention (week 8)

Assessed with dual-EEG, with the Phase Locking Value (PLV) in the alpha band frequency (6-9 Hz) during the free play task. We expect that neural synchrony between mother and infant will increase (more) in the intervention group.

Secondary Outcomes

  • Change from baseline worry(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline mindfulness skills(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline postpartum-specific anxiety(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline infant temperament(Before the intervention (baseline, week 0), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline parenting self-efficacy(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline personal goal(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline self-compassion(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline bonding(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))
  • Change from baseline mindful parenting(before the intervention (baseline, week 0), halfway through the intervention (week 4), post-intervention (week 8) and after 10-weeks follow-up (week 18))

Study Sites (1)

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