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Visual Aid for Induced Birth (VAIL Trial)
N/A
Recruiting
Research Sponsored by Washington University School of Medicine
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 10 minutes (during completion of survey)
Awards & highlights
Summary
This trial seeks to create a visual aid tool that meets the needs of pregnant women, to help them feel more informed and satisfied with induction methods.
Who is the study for?
This trial is for English-speaking pregnant women scheduled for or admitted to labor induction, without major fetal anomalies, chromosomal issues, prior cesarean sections, already started inductions, terminations via induction, or fetal growth restrictions with doppler abnormalities.
What is being tested?
The study is testing a new visual aid tool designed to educate about labor induction. It's based on input from historically marginalized pregnant women and aims to see if it improves their knowledge, satisfaction, and trust in doctors regarding induction methods.
What are the potential side effects?
Since the intervention involves educational material rather than medication or medical procedures, there are no direct physical side effects expected from the visual aid itself.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 10 minutes (during completion of survey)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~10 minutes (during completion of survey)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Induction of labor knowledge
Secondary study objectives
Patient satisfaction
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Visual aid counselingExperimental Treatment1 Intervention
Counseling on induction of labor with either a video or a handout
Group II: Standard counselingActive Control1 Intervention
Standard induction of labor counseling
Find a Location
Who is running the clinical trial?
Washington University School of MedicineLead Sponsor
1,970 Previous Clinical Trials
2,308,539 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My treatment has already started.I have a known genetic abnormality.I am currently undergoing induction termination.
Research Study Groups:
This trial has the following groups:- Group 1: Standard counseling
- Group 2: Visual aid counseling
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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