The Effect of an mHealth Mindfulness Program on the Well-being of Pregnant Women Diagnosed with High-Risk Pregnancy Receiving Outpatient Care

Effects of an mHealth Mindfulness Program for High-Risk Pregant Women in the Community

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010281

Enrollment

Registered

2025-03-11

Start date

2025-03-24

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : If participants decide to take part in this study, they will complete an online consent form and install the developed app. Participants will be assigned to either the experimental group

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: ? Aged 19 years or older ? Pregnant women who are between 14 weeks and 32 weeks of gestation and can feel fetal movements ? Pregnant women diagnosed with any of the following 19 high-risk pregnancy conditions and currently receiving outpatient care ? Preterm labor, delivery-related bleeding, severe preeclampsia, premature rupture of membranes, placental abruption, placenta previa, imminent miscarriage, polyhydramnios, oligohydramnios, antepartum bleeding, cervical insufficiency, (gestational) hypertension, multiple pregnancy, (gestational) diabetes, hyperemesis gravidarum with metabolic disorders, kidney diseases, heart failure, intrauterine growth restriction, and uterine and adnexal diseases ? Pregnant women diagnosed with high-risk pregnancies due to pre-pregnancy hypertension, diabetes, stillbirth, or a history of preterm birth before 34 weeks, and currently receiving outpatient care. ? Pregnant women who can install and use the app on a smartphone ? Pregnant women who have not previously participated in mindfulness meditation ? Pregnant women with no history of psychiatric disorders and who are not currently taking related medications ? Pregnant women who fully understand the research purpose and have consented to participate in the study online ? Pregnant women who can understand and respond to the survey content

Exclusion criteria

Exclusion criteria: ? Pregnant women who give birth before the end of the study ? Pregnant women who are exposed to severe stress during the study period ? Pregnant women who do not follow the study guidelines and procedures ? Married migrant women and foreign pregnant women (may have difficulty with communication due to language barriers) ? Pregnant women who have difficulty reading and understanding Korean

Design outcomes

Primary

Measure	Time frame
depression;happiness	—

Secondary

Measure	Time frame
pregnancy stress;anxiety;maternal-fetal attachment	—

Countries

Korea, Republic of

Contacts

Public ContactHyunkyung Choi

Kyungpook National University

hchoi@knu.ac.kr+82-53-950-4484

Outcome results