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NCT06841367Not yet recruiting

The Effect of Awareness-Based Stress Reduction Training on Preeclampsia and Anxiety

The Effect of Awareness-Based Stress Reduction Training on Anxiety Level and Physiological Parameters in Pregnant Women Diagnosed With Preeclampsia

Source: ClinicalTrials.gov · Last updated 24 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Preeclampsia is a multisystem disease that occurs during pregnancy and carries risks into the postpartum period. This condition, which threatens maternal and fetal health, requires close monitoring and good care. Pregnant women need to rely on both their previously used coping mechanisms and learn new coping methods to manage the stress associated with high-risk pregnancies. Complementary and integrative therapies are utilized in managing hypertensive disorders and anxiety during pregnancy. Literature reviews show that complementary medicine practices included in current care may be effective in alleviating the symptoms of preeclampsia and reducing anxiety levels. However, the existing scientific studies are not at a sufficient level of evidence, and more advanced studies are needed in this area. The aim of our thesis study is to examine the effect of mindfulness-based stress reduction training on anxiety levels and physiological parameters in pregnant women diagnosed with preeclampsia.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
18 Feb 2025
Start date
1 Mar 2025
Primary completion date
5 May 2025
Lead sponsor
Istanbul University - Cerrahpasa
NCT number
NCT06841367

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 1 Mar 2025 to the primary completion date, 5 May 2025
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Having any additional disease other than preeclampsia

Other

  • Participant's voluntary withdrawal from the study
  • Having a cesarean section for any reason

Who the study is looking for

  • Knowing Turkish
  • Being literate
  • Being over 18
  • Being primiparous
  • Having a singleton fetus and cephalic presentation
  • Being diagnosed with preeclampsia
  • Agreeing to participate in the study

Age in the registry: 18 years to 35 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.