The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve.
Recruiting
N/A
Interventional Study
Induction of Labor Affected Fetus / Newborn
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 180 (estimated)
- Sponsor
- Wolfson Medical Center · Government
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About This Trial
To determine whether watching a personalized video prior to medically indicated labor induction among term parturients reduces anxiety levels according to the STAI questionnaire, compared to a standard counselling.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant women, aged 18-45, undergoing medical IOL at term.
* Unfavorable cervix (BISHOP score \<6).
* Cervical ripening with either prostaglandin E2 (PGE2) tablets or extra-amniotic balloon (EAB).
* Provided consent to participate in the study.
* No language barrier preventin…
Contacts