Recruiting NA Induction of Labor Affected Fetus / Newborn

New treatment option for Induction of Labor Affected Fetus / Newborn

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

ClinicalTrials.gov ID: NCT06375746

What this study is testing

What it's testing
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.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 45, women only. Healthy volunteers may be eligible.

You may be able to join if

  • 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.

You likely can't join if

  • Sensitivity to PGE2.
  • Preterm labor.
  • Premature rupture of membranes.
  • Stillbirth.
  • Elective pregnancy termination.

The study team makes the final eligibility decision.

Where it's taking place

  • Holon, Israel

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling female, 18 years to 45 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Holon, Israel. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.