RecruitingNot Applicable

The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve.

Israel180 participantsStarted 2024-05-01

Plain-language summary

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 can participate

Age range18 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

STAI questionnaire score

Timeframe: Patient in both the study and the control groups will be asked to complete the STAI questionnaire twice as detailed below: • Prior to labor induction • After completion of IOL (either immediately after insertion of EAB or first PGE2 tablet).

Trial details

NCT IDNCT06375746

SponsorWolfson Medical Center

Sponsor typeOTHER_GOV

Study typeINTERVENTIONAL

Primary completion2024-08-01

Contact for this trial

Matan Friedman, MD

+972544210360 matan.friedman@gmail.com

View on ClinicalTrials.gov More Induction of Labor Affected Fetus / Newborn trials