Evaluating how mothers perceive fetal movements using computerized monitoring.
Maternal Perception of Fetal Movements Evaluation Using and Analyzing the Variables of Antepartum Computerized Cardiotocography: An Exploratory Study.
This study is testing how well mothers can feel their baby's movements and if that matches up with the baby's health as measured by a special monitoring device.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 51 (estimated) |
| Ages | 18 Years to 48 Years |
| Sex | Female |
| Sponsor | University of Campania Luigi Vanvitelli Academic / other |
| Locations | 1 site (Napoli, Italia) |
| Trial ID | NCT04397874 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the relationship between maternal perception of fetal movements and fetal well-being as measured by computerized cardiotocography (cCTG). It focuses on non-laboring term singleton pregnancies to assess how accurately mothers can perceive fetal activity and how this correlates with cCTG parameters. By analyzing these variables, the study seeks to enhance understanding of fetal health indicators and maternal awareness during pregnancy.
Who should consider this trial
Good fit: Ideal candidates for this study are women with non-laboring term singleton pregnancies between 37 and 41 weeks of gestation.
Not a fit: Patients with fetal malformations, stillbirths, or preterm deliveries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve maternal awareness of fetal well-being, potentially leading to better monitoring and outcomes for pregnancies.
How similar studies have performed: While there have been studies on fetal movement counting and perinatal outcomes, this specific approach of correlating maternal perception with cCTG parameters is novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * nonlaboring term singleton pregnancies (37 0/7 - 41 6/7 weeks of gestation) Exclusion Criteria: * fetal malformations, stillbirths, preterm deliveries
Where this trial is running
Napoli, Italia
- Università degli studi della Campania "Luigi Vanvitelli"- OB & Gyn - — Napoli, Italia, Italy (Recruiting)
Study contacts
- Study coordinator: Marco La Verde, MD
- Email: dr.marcolaverde@gmail.com
- Phone: +393389412266
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.