Using a personalized video to reduce anxiety before labor induction
The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve - a Randomized Controlled Trial
This study tests if watching a personalized video before labor induction can help pregnant women feel less anxious about the process.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 180 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | Female |
| Sponsor | Wolfson Medical Center Government |
| Locations | 1 site (Holon) |
| Trial ID | NCT06375746 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate whether watching a customized informative video prior to medically indicated labor induction can reduce anxiety levels in pregnant women. Participants will be assessed using the STAI questionnaire to measure anxiety before and after the intervention. The study focuses on women with an unfavorable cervix who are undergoing labor induction using either prostaglandin E2 or an extra-amniotic balloon. By providing tailored information about the induction process, the study seeks to enhance patient engagement and alleviate concerns regarding maternal and fetal health.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women aged 18-45 who are undergoing medical induction of labor at term with an unfavorable cervix.
Not a fit: Patients who are experiencing preterm labor, have a sensitivity to PGE2, or have other complications such as stillbirth or premature rupture of membranes may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety levels in women undergoing labor induction, leading to a more positive birth experience.
How similar studies have performed: Previous studies have indicated that providing more information and options to women undergoing labor induction can improve their experience, suggesting that this approach may be beneficial.
Eligibility criteria
Show full inclusion / exclusion 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 preventing completion of the questionnaire. Exclusion Criteria: * Sensitivity to PGE2. * Preterm labor. * Premature rupture of membranes. * Stillbirth. * Elective pregnancy termination.
Where this trial is running
Holon
- Wolfson Medical Center — Holon, Israel (Recruiting)
Study contacts
- Study coordinator: Matan Friedman, MD
- Email: matan.friedman@gmail.com
- Phone: +972544210360
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.