Recruiting

Mindfulness-Based Postpartum Education Impact on Maternal Role Perception and Anxiety Levels

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Study Aim

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.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Mental Disorders

+ Anxiety Disorders

Over 18 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: July 2026
See protocol details

Summary

Principal SponsorTokat Gaziosmanpasa University
Study ContactDamlagul ACAR, MSc StudentMore contacts
Last updated: July 14, 2026
Sourced from a government-validated database.Claim as a partner

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.

Principal SponsorTokat Gaziosmanpasa University
Study ContactDamlagul ACAR, MSc StudentMore contacts
Last updated: July 14, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

84 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Mental DisordersAnxiety Disorders

Criteria

7 inclusion criteria required to participate
Mothers living in the same home environment with their baby

Mothers who are in the postpartum ward within the first 24 hours after delivery

Mothers who can read and understand Turkish and fully complete the questionnaires

Mothers whose health status is suitable to participate in the education process

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5 exclusion criteria prevent from participating
Mothers whose newborns are admitted to the intensive care unit or have serious health problems

Mothers who have previously participated in a mindfulness-based education or therapy program

Mothers who incompletely fill out the questionnaires or do not participate in the post-test phase

Mothers who cannot participate regularly in the education process or maintain communication during the follow-up period

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

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

Recruiting

Tokat Gaziosmanpasa University University Hospital

Tokat Province, Turkey (Türkiye)Open Tokat Gaziosmanpasa University University Hospital in Google Maps
Recruiting
One Study Center