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NCT07451418

The Effect of Mindfulness Compassionate Living Training on Unwanted Pregnancies

Not yet recruiting NA Last updated 5 March 2026
What this trial tests

NA trial testing Session 1: How We Evolved - Threat, Impulse, and Soothing Systems in Mindfulness Compassionate Living Training in 68 participants. Not yet recruiting.

Timeline
15 March 2026
Primary endpoint
15 June 2026
15 August 2026

Quick facts

Lead sponsorAtaturk University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposesupportive care
Enrollment68
Start date15 March 2026
Primary completion15 June 2026
Estimated completion15 August 2026

Drugs / interventions tested

Conditions studied

Sponsor

Ataturk University

Who can join

Adults 18 to 45, female only, with Mindfulness Compassionate Living Training. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will be conducted as a single-blind, randomized controlled trial with pregnant women who do not want or plan a pregnancy and do not intend to terminate it, and who apply for pregnancy examination at the Obstetrics and Gynecology outpatient clinic of a training and research hospital in Turkey. Data will be collected at the Obstetrics and Gynecology outpatient clinic of the Training and Research Hospital in Ağrı between March 2026 and June 2026. The study population will consist of pregnant women aged 18 to 45 who apply to the Obstetrics and Gynecology outpatient clinic during the specified period, and who have an unwanted or unplanned pregnancy. The sample size was calculated using the GPower computer program. Using power analysis at the α=0.05 level, the effect size was calculated as 150, 153 (d=0.8) and the study power as 90%, indicating that at least 68 pregnant women should be included in the sample. Pregnant women who meet the research criteria and agree to participate in the study will be randomly assigned to an experimental group and a control group. The study will use a pregnancy profile form prepared by the researcher in accordance with the literature, containing socio-demographic data of pregnant women who applied to the Obstetrics and Gynecology outpatient clinic; the Self-Acceptance Scale for Pregnant Women (SAPS) to determine the pregnant woman's level of self-acceptance; the Depression, Anxiety, and Stress Scale (DASS-21) to evaluate the symptoms of depression, anxiety, and stress; and the Self-Compassion Scale Short Form (SCI-S) to evaluate self-compassion.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Session 1: How We Evolved - Threat, Impulse, and Soothing Systems

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