RECRUITINGINTERVENTIONAL
The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve.
The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve - a Randomized Controlled Trial
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.
Who May Be Eligible (Plain English)
Who May Qualify:
- 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 preventing completion of the questionnaire.
Who Should NOT Join This Trial:
- Sensitivity to PGE2.
- Preterm labor.
- Premature rupture of membranes.
- Stillbirth.
- Elective pregnancy termination.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
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 preventing completion of the questionnaire.
Exclusion Criteria:
* Sensitivity to PGE2.
* Preterm labor.
* Premature rupture of membranes.
* Stillbirth.
* Elective pregnancy termination.
Treatments Being Tested
OTHER
Personalized video
After enrollment and assignment to the intervention group, patients will receive a link to a personalized video describing the different induction methods by a text message.
Locations (1)
Wolfson Medical Center
Holon, Israel