Mindfulness-Based Postpartum Education Impact on Maternal Role Perception and Anxiety Levels
This study aims to observe how mindfulness-based postpartum education impacts new mothers' perception of their maternal role and their anxiety levels, using a specific evaluation scale.
Data Collection
Collected from today forward - ProspectiveMental Disorders
+ Anxiety Disorders
Case-Control
Comparing exposures between individuals with and without disease in order to identify potential risk factors.Summary
Study start date: July 9, 2026
Actual date on which the first participant was enrolled.This research focuses on understanding how mindfulness-based education given to new mothers before they leave the hospital can impact their view of their maternal role and their anxiety levels. The study takes place at Tokat Gaziosmanpaşa University Research and Practice Hospital's Obstetrics and Gynecology Clinic, involving 84 new mothers, half of whom will receive the mindfulness education (experimental group), and the other half will not (control group). The goal is to see if this special education can help new mothers feel more confident in their role and less anxious, ultimately improving their overall well-being and care for their newborn. In the first 24 hours after giving birth, the experimental group will receive a 60-minute mindfulness education session in addition to the usual hospital discharge care. The control group will only receive the standard hospital discharge education. One week later, both groups will be evaluated. The experimental group will also receive weekly reminders and follow-ups via WhatsApp for a month. At the end of the first month postpartum, a final evaluation will be conducted. The study uses a Maternal Role Perception Scale to measure the mothers' view of their maternal role, with higher scores indicating a better and more developed perception. The potential benefits include improved maternal role perception and reduced anxiety levels, contributing to better postpartum care.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.84 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Case-Control
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Tokat Gaziosmanpasa University University Hospital
Tokat Province, Turkey (Türkiye)Open Tokat Gaziosmanpasa University University Hospital in Google Maps