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Investigating the effect of mindfulness on preeclampsia

Investigating the impact of midwifery counseling and mindfulness-based stress reduction on pregnancy outcomes in women with preeclampsia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240128060834N1
Enrollment
80
Registered
2024-04-07
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

??? ?????? ?????? ??? ????????. Mild to moderate pre-eclampsia

Interventions

Intervention 1: Intervention group: 21-30 weeks pregnant women suffering from pre-eclampsia who meet the criteria to enter the research and are referred to the selected medical centers of Qazvin city

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Suffering from mild to moderate preeclampsia 2. Single and live fetus 3. Pregnancy age between 21 and 30 weeks (based on LMP and ultrasound of the first trimester of pregnancy) 4. Having minimum literacy in reading and writing 5. Consent to participate in the study 6. Living in Qazvin province

Exclusion criteria

Exclusion criteria: 1. Suffering from chronic physical diseases (cardiovascular, renal, autoimmune, diabetes) 2. Obstetric problems other than preeclampsia (severe nausea and vomiting of pregnancy, placenta previa, etc.) 3. Drug addiction 4. Suffering or having a history of suffering from mental illnesses, psychological treatments, and the use of nerve drugs, the existence of a stressful situation for the participant in the past 6 months, such as (death of first-degree relatives, etc.) 5. Suffering from acute diseases during the fetal period (genetic problems, hydrocephalus, etc.)

Design outcomes

Primary

MeasureTime frame
Maternal outcomes. Timepoint: During pregnancy and after delivery. Method of measurement: Changes in systolic and diastolic blood pressure, gestational age at delivery,.;Neonatal outcomes. Timepoint: after delivery. Method of measurement: Apgar score of the baby at delivery, weight, head circumference and height of the baby at delivery.

Secondary

MeasureTime frame
Average stress score in women with preeclampsia. Timepoint: Before and after the intervention. Method of measurement: Cohen's Perceived Stress Questionnaire (PSS-14).;Average score of Mindfulness in women with preeclampsia. Timepoint: Before and after the intervention. Method of measurement: Freiburg Mindfulness Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Haji Moulaei

Shahroud University of Medical Sciences

miss.n.h.6517@gmail.com+98 23 3239 1850

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026