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Behavioral Intervention
Post-intervention for Pregnancy (BELIEVE Trial)
N/A
Waitlist Available
Led By Alison Stuebe, MD, MSc
Research Sponsored by University of North Carolina, Chapel Hill
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Healthcare Team Participants
* Employed as one of the following roles: maternity care provider, nurse, lactation consultant or doula.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (pre-intervention) and after completing the ipc training intervention, a total of up to 4 months
Awards & highlights
Summary
This is a step-wedge design implementation protocol of an interprofessional education curriculum intervention that is delivered through virtual reality and designed to reduce disparities and improve patient experiences in receiving maternal healthcare.
Eligible Conditions
- Pregnancy
- Postpartum
- Pain
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline (pre-intervention) and after completing the ipc training intervention, a total of up to 4 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (pre-intervention) and after completing the ipc training intervention, a total of up to 4 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Severe Postpartum Pain
Secondary study objectives
Acetaminophen doses administered
Birthing parent-reported experiences of the respectful care (Qualitative)
Feasibility of the IPC training
+7 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: Post-interventionActive Control1 Intervention
In the post-intervention sequence(s), birthing people at participating hospitals will experience treatment by health care teams that have undergone the Building Equitable Linkages With Interprofessional Education Valuing Everyone interprofessional education (BELIEVE IPE) training.
Group II: Pre-interventionPlacebo Group1 Intervention
In the pre-intervention sequence(s), birthing people at participating hospitals will experience treatment-as-usual.
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Who is running the clinical trial?
American Heart AssociationOTHER
343 Previous Clinical Trials
4,939,729 Total Patients Enrolled
University of North Carolina, Chapel HillLead Sponsor
1,543 Previous Clinical Trials
4,209,082 Total Patients Enrolled
Alison Stuebe, MD, MScPrincipal InvestigatorUniversity of North Carollina at Chapel Hill
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