Comparing two methods for monitoring fetal movements and their impact on maternal mental health
The Effect of Two Different Self-Assessment Methods for Fetal Movement Monitoring on Maternal Psychosocial Status
This study is testing two different ways for pregnant women to track their baby's movements to see which one helps them feel more connected to their baby and less stressed.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 76 (estimated) |
| Sex | Female |
| Sponsor | Kırklareli University Academic / other |
| Locations | 1 site (Kırklareli, Center) |
| Trial ID | NCT06558162 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effects of two different self-assessment methods for monitoring fetal movements, namely the Mindfetalness method and the Sadovsky method, on the psychosocial status of pregnant women. The Mindfetalness method emphasizes the quality of fetal movements, encouraging mothers to focus on the nature and strength of movements rather than just counting them. The study aims to determine which method may enhance maternal-fetal attachment and reduce stress during pregnancy. Participants will be monitored between 28-32 weeks of gestation, and their experiences will be assessed to identify potential benefits for maternal mental health.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women over 18 years old, experiencing a single pregnancy between 28-32 weeks of gestation, and who are first-time mothers.
Not a fit: Patients with chronic or psychiatric illnesses, or those with high-risk pregnancies, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve maternal mental health and enhance the bonding experience between mothers and their unborn babies.
How similar studies have performed: While there are studies on fetal movement monitoring, this specific comparison of self-assessment methods is novel and has not been previously explored.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Volunteering to participate in the research * Over 18 years of age * Single pregnancy * Being between 28-32 weeks of gestation * Primiparity * At least primary school graduation * No diagnosed problems related to the health of the fetus (such as fetal anomaly, intrauterine growth retardation) No risky pregnancy (such as pre-eclampsia, diabetes, heart disease, placenta previa, oligohydramnios) Exclusion Criteria: * Not having any disabilities that may prevent communication (speech, hearing, mental) * No chronic or psychiatric illness * Conception with assisted reproductive techniques
Where this trial is running
Kırklareli, Center
- Neriman Güdücü — Kırklareli, Center, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Aleyna Yıldız, Midwife
- Email: aleynayldz10@gmail.com
- Phone: 05077136955
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.