An Informative Video Before Planned External Cephalic Version
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Video.
- Who it may be relevant to
- Registry conditions: Breech Presentation. Basic parameters: 18 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Israel
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
An Informative Video Before Planned External Cephalic Version - Does it Reduce Maternal Anxiety and Improve Chances of Success? - a Randomized Control Trial
Overview
A randomized control trial to investigate whether an informative video before planned external cephalic version reduces maternal anxiety and improves chances of success.
Detailed description
Women with a breech presentation scheduled to undergo an external cephalic version that meet the criteria are recruited in the Emergency Room by offering every woman that is scheduled to undergo an external cephalic version to participate. Women who agree to participate are asked to sign an inform consent, and are randomized to intervention group and control group. In the Emergency Room sonographic data is collected including amniotic fluid index, engaged presenting part, sonographic and clinical estimation of fetal weight, place of the placenta and various angles between the fetus and the bladder (These data are collected for the study). All participants in the intervention group watches an informative video on recruitment. This video describes in detail the expected external cephalic version process.
Before the external cephalic version and an hour after a successful or an unsuccessful external cephalic version the situation-specific anxiety is measured using the State-Trait Anxiety Inventory score (Attached).
Interventions
- Other Video
All participants in the intervention group watches an informative video on recruitment. This video describes in detail the expected external cephalic version process.
Primary outcome measures
- higher success rates. [Time frame: 4 years]
Secondary outcome measures (1)
- impact of watching an informative video before external cephalic version on maternal anxiety levels [Time frame: 4 years]
Eligibility criteria
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…
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Israel · 1 center
- Meir Medical Center — Kfar Saba
Identifiers
NCT: NCT06187948 · 0214-22