An Informative Video Before Planned External Cephalic Version
Recruiting · NCT06187948 · Interventional (participants receive a specific treatment) · Lead sponsor: Meir Medical Center
View the official record on ClinicalTrials.gov →Interventions studied
Video
What this trial is about
A randomized control trial to investigate whether an informative video before planned external cephalic version reduces maternal anxiety and improves chances of success.
Who can take part
Age range
18 Years to 45 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Women between ages 18-45
- with a singleton gestation
- at gestational week of 36 weeks 0 days until 38 weeks 0 days
- who admitted labor word for external cephalic version .
Exclusion criteria
- Women who had a past cesarean section
- Women with oligohydramnios (Amniotic fluid index \< 5 cm)
- Women who had a past external cephalic version
- Women with a failed external cephalic version in current pregnancy
- Women who take medication for depression/anxiety disorders
- Women with a complicated pregnancy including fetal anomalies, polyhydramnios…
Where it is running
1 location listed.
- Meir Medical Center - Kfar Saba, Israel