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Mediation / Mindfulness stress reduction program group / Depression · Interventional Study
ClinicalTrials.gov · August 11, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a completed but unpublished trial registration documenting a planned randomized controlled trial of mindfulness-based stress reduction in 108 pregnant women. No results are posted in this registry record. The reader cannot assess efficacy, safety, or any clinical outcome until results are published.
Interventional, Randomized, Parallel, Open label, Treatment purpose. Pregnancy Related, Mediation, Depression, Maternal-Fetal Relations; Female; age from 20 Years; to 35 Years; accepts healthy volunteers. Intervention: Mindfulness Group. Compared with: Control Group — No Intervention. n = 108. 1 site: Turkey (Türkiye).
This is a completed but unpublished trial registration documenting a planned randomized controlled trial of mindfulness-based stress reduction in 108 pregnant women. No results are posted in this registry record. The reader cannot assess efficacy, safety, or any clinical outcome until results are published.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
This is a completed registry record with no results posted; the study design is sound (RCT, n=108) but no outcomes are reported, making it a planning document only.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT05804838). This is a study registration, not published results. Lead sponsor: Uskudar University. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 108 participants (ACTUAL). Conditions: Pregnancy Related, Mediation, Depression, Maternal-Fetal Relations. Interventions: OTHER: Mindfulness stress reduction program group. Primary outcome measures: Psychological well-being scale , at inclusion; Beck depression scale , at inclusion; Prenatal attachment scale , at inclusion; Conscious awareness scale , at inclusion. Brief summary: This study was planned to examine the effects of the Mindfulness-Based Stress Reduction Program, which is one of the popular concepts of the 21st century, on depression, psychological well-being and prenatal attachment, which are likely to occur as a result of increased stress during an important period that requires adjustment as a result of physical, mental and cognitive changes during pregnancy. It will be conducted in a randomized parallel controlled experimental design type using Consolidated Standards of Reporting Trials (CONSORT) guidelines. It is planned to be carried out with the ZOOM Cloud Meetings program, which is an online education platform, with pregnant women who apply to the Health Sciences University Ümraniye Training and Research Hospital pregnancy polyclinic in the Ümraniye district of Istanbul. The universe of the research will be the pregnant women who applied to the Health Sciences University Ümraniye Training and Research Hospital pregnant outpatient clinic. Primiparous pregnant women who meet the inclusion criteria and willingly agree to participate in the study will be included in the study. 54 people in the intervention group, 54 people in the control group, and a total of 108 people will be taken. While the Conscious Awareness-Based Stress Reduction Program adapted for pregnant women will be applied to the intervention group, routine follow-up will be applied to the control group within the scope of the outpatient clinic follow-up of the relevant institution. Informed Voluntary Consent Form, Descriptive Characteristics Information Form, Psychological Well-Being Scale, Beck Depression Scale, Prenatal Attachment Scale and Conscious Awareness Scale will be administered to the participants included in the study. As a result of the findings, the discussion and results of the study will be written.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.