RecruitingNot Applicable

Mindfulness-Based Postpartum Discharge Education on Maternal Role and Anxiety

Turkey (Türkiye)84 participantsStarted 2026-07-09

Plain-language summary

This study will be conducted as a quasi-experimental research with a pretest-posttest control group design at the Obstetrics and Gynecology Clinic of Tokat Gaziosmanpaşa University Research and Practice Hospital, aiming to evaluate the effects of mindfulness-based postpartum discharge education on mothers' maternal role perception and anxiety levels. The sample will consist of 84 postpartum women (42 in the experimental group and 42 in the control group) who meet the inclusion criteria, determined through G\*Power analysis. Stratified randomization will be used for group allocation. Data will be collected using a Personal Information Form, the Maternal Role Perception Scale, and the Postpartum Specific Anxiety Scale. Within the first 24 hours postpartum (baseline/pretest), the experimental group will receive a 60-minute individual "Mindfulness-Based Postpartum Education Program" administered by the researcher in addition to routine discharge care, while the control group will receive only standard hospital discharge education. One week after the education, a second measurement will be applied to both groups. Subsequently, the experimental group will be systematically followed up for one month via WhatsApp with weekly reminder messages and monitoring charts. At the end of the first postpartum month (30th day), the final posttest measurements will be completed. The effects of the education over repeated time points will be analyzed using SPSS 22.0 software with descriptive statistics, parametric tests (Independent/Paired Sample t-test, repeated measures Two-Way ANOVA, Pearson correlation), and non-parametric tests (Mann Whitney U, Wilcoxon, Spearman correlation) at a significance level of 0.05.

Who can participate

Age range

18 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Mothers aged 18 and older who voluntarily agree to participate in the study * Mothers who have had a healthy singleton birth * Mothers who are in the postpartum ward within the first 24 hours after delivery * Mothers living in the same home environment with their baby * Mothers who can read and understand Turkish and fully complete the questionnaires * Mothers who can use mobile communication tools (e.g., WhatsApp) * Mothers whose health status is suitable to participate in the education process Exclusion Criteria: * Mothers with serious physical or psychiatric illnesses in the postpartum period * 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 cannot participate regularly in the education process or maintain communication during the follow-up period * Mothers who incompletely fill out the questionnaires or do not participate in the post-test phase

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Maternal Role Perception

Timeframe: Within the first 24 hours postpartum (baseline), at 1 week postpartum, and at 1 month postpartum.

Trial details

NCT IDNCT07702058

SponsorTokat Gaziosmanpasa University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-09-09

Contact for this trial

Damlagul ACAR, MSc Student

+90 552 829 30 11 damlagul.acar7825@gop.edu.tr

View on ClinicalTrials.gov More Postpartum Period trials