CClinicalTrials.gg
CompletedNCT03917745Updated Jul 14, 2022

E-health Intervention in Women With Pregnancy Distress

An interventional study of eHealth mindfulness intervention in Pregnancy Distress, sponsored by Tilburg University. Completed at 1 site in Netherlands. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-07-14.

Sponsored by Tilburg University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
219
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

The study aims to reduce the levels of distress (depression and anxiety) during pregnancy. The study investigates the effectiveness of an eHealth pregnancy distress-reducing mindfulness training in women with pregnancy distress.

Read the detailed description

During pregnancy, women are at risk for mental health problems: up to 20% present with distress symptoms (depression and/or anxiety). Apart from the adverse effects on the woman herself, pregnancy distress negatively affects pregnancy outcome, infant health, postpartum mother-child interaction and child development.

Mindfulness-based interventions are a type of intervention that is increasingly being used to treat symptoms of stress, anxiety and depression. They are cheap and accessible to the whole population.

Current study aims to examine the effectiveness of a mindfulness training to reduce distress during pregnancy. Women who score above cut off on the Edinburgh Depression Scale (EDS) and Tilburg Pregnancy Distress Scale (TPDS) at 12 weeks of gestation, will be randomly allocated to the intervention or control group. Women in the intervention group will be contacted and invited to participate in the mindfulness-based intervention, which consists of 8 weeks of internet mindfulness training. The control group will receive care as usual.

The primary outcome of the study is: Does the mindfulness internet training "Ontspannen zwanger", offered during pregnancy, reduce pregnancy distress, compared to care as usual? The secondary outcome is: Does the mindfulness internet training result in better mindfulness skills?

02

Conditions studied

  • Pregnancy Distress

Keywords

  • anxiety
  • depression
  • eHealth
  • mindfulness
  • pregnancy distress
03

In context

Lead sponsor

Tilburg University is the lead sponsor of 27 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Pregnant women (18+y) who have their first antenatal visit \< 12 weeks;
  • Score above cut off on the Edinburgh Depression Scale (EDS) and Tilburg Pregnancy Distress Scale (TPDS) at 12 weeks of gestation;
  • Dutch-speaking or understanding Dutch.

Exclusion criteria

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);
  • HIV;
  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
219 participants (actual)

Study arms

  • Experimental
    eHealth mindfulness intervention group

    8 weeks of internet mindfulness training

    Behavioral: eHealth mindfulness intervention

  • No intervention
    Control group

    Care as usual

Interventions

  • BehavioraleHealth mindfulness intervention

    The web-based intervention consists of eight sessions including psycho-education about the mechanisms of stress, coping and relaxation, especially related to pregnancy, practicing mindfulness skills (i.e. mindful breathing, mindful moving, observing and letting-go of thoughts and emotions with a non-judgmental attitude), sharing experiences, and doing home assignments. The sessions have been developed specifically for pregnant women and acknowledge pregnancy-related distress. An online coach will review questions and home assignments of the participants. Women will start the training at 16 weeks gestation.

    Also known as: Ontspannen zwanger

06

What researchers measure

Primary outcomes

  1. Depressive symptoms

    Measured by the 10-item Edinburgh Depression Scale (EDS). The EDS is the most widely used self-rating scale to assess depressive symptoms in the perinatal period. It consists of ten items and three sub-scales: anhedonia, anxiety and depression. The questionnaire has been validated in Dutch pregnant women. The EDS total score ranges from 0 to 30, with higher scores indicating more depressive symptoms.

    Time frame: Difference between the intervention group en the control group, measured at 28 weeks (after the intervention).

Secondary outcomes

  1. Negative Affect

    Measured by a subscale of the Tilburg Pregnancy Distress Scale (TPDS): Negative Affect, which consists of 10 items. The TPDS has been validated among Dutch pregnant women and it is a reliable measure to assess pregnancy-related emotional distress. The total score ranges from 0 to 30, with higher scores indicating more emotional distress symptoms.

    Time frame: Difference between the intervention group en the control group, measured at 28 weeks (after the intervention).

Other outcomes

  1. Mindfulness skills

    Measured by three facets of the Five Facet Mindfulness Questionnaire Short Form (FFMQ-3-SF): acting with awareness, non-judging and non-reacting, which consists of 15 items. The validity of the measure is established and indices of internal reliability were found to be adequate. The total score ranges from 0 to 60, with higher scores indicating better mindfulness skills.

    Time frame: Measured in the intervention group, the difference between 16 weeks (before the intervention) and 28 weeks (after the intervention).

  2. Rumination

    Measured by the Rumination-Reflection Questionnaire (RRQ), which consists of 12 items and is a validated and reliable instrument. The score ranges from 0 to 48, with higher scores indicating more rumination.

    Time frame: Measured in the intervention group, the difference between 16 weeks (before the intervention) and 28 weeks (after the intervention).

  3. Self compassion

    Measured by the Self Compassion Scale Short Form (SCS-SF), which consists of 12 items, and is a validated and reliable measure. The total score ranges from 0 to 72, with higher scores indicating higher self compassion.

    Time frame: Measured in the intervention group, the difference between 16 weeks (before the intervention) and 28 weeks (after the intervention).

07

Study locations

1 site
  • Tilburg University
    Tilburg, Netherlands
08

References and documents

Publications

  • Hulsbosch LP, Nyklicek I, Potharst ES, Meems M, Boekhorst MGBM, Pop VJM. Online mindfulness-based intervention for women with pregnancy distress: design of a randomized controlled trial. BMC Pregnancy Childbirth. 2020 Mar 13;20(1):159. doi: 10.1186/s12884-020-2843-0. PubMed 32169030 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03917745
Lead sponsor
Tilburg University
Responsible party
prof.dr. Victor J Pop (Principal Investigator, Tilburg University) — Principal investigator
First posted
Apr 17, 2019
Start date
Aug 12, 2019
Primary completion
Jun 16, 2022
Completion
Jun 16, 2022
Last update
Jul 14, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion