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Prenatal Counseling for Postpartum Health

N/A
Waitlist Available
Led By Eleanor Bimla Schwarz, MD, MS
Research Sponsored by University of California, Davis
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Aged 18-40 years
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months postpartum
Awards & highlights

Study Summary

This trial will help determine if either of these interventions leads to improved maternal health outcomes.

Who is the study for?
This trial is for pregnant women aged 18-40, fluent in English, expecting one baby between 27-37 weeks along, born in the US, with access to a text-capable phone and internet. It's not for those with multiple babies, HIV or breastfeeding contraindications, past certain breast surgeries, using assisted reproduction like IVF.Check my eligibility
What is being tested?
The study compares two counseling interventions during pregnancy: one focuses on benefits of breastfeeding for mothers' health; the other emphasizes advantages of having smoke-free homes. Women are randomly assigned to either group and followed up until at least six months postpartum.See study design
What are the potential side effects?
Since this trial involves counseling rather than medical treatments or drugs, there are no direct physical side effects expected from participating. However, emotional or psychological responses to the content discussed cannot be entirely predicted.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am between 18 and 40 years old.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months postpartum
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 months postpartum for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Duration of breastfeeding
Secondary outcome measures
Duration of any breastfeeding or pumping at 24 months postpartum
Knowledge of the maternal health benefits of lactation
Smoke-free home policy

Trial Design

2Treatment groups
Active Control
Group I: Counseling about the Maternal Benefits of BreastfeedingActive Control1 Intervention
Participants will review a slide deck while receiving scripted counseling designed to increase understanding of the maternal health benefits of breastfeeding.
Group II: Counseling about the benefits of Smoke-free HomesActive Control1 Intervention
Participants will review a slide deck while receiving scripted counseling designed to increase understanding of the health benefits of smoke free homes.

Find a Location

Who is running the clinical trial?

Health Resources and Services Administration (HRSA)FED
84 Previous Clinical Trials
151,036 Total Patients Enrolled
University of California, DavisLead Sponsor
910 Previous Clinical Trials
4,706,540 Total Patients Enrolled
1 Trials studying Maternal Care Patterns
60 Patients Enrolled for Maternal Care Patterns
Eleanor Bimla Schwarz, MD, MSPrincipal InvestigatorUC Davis Health

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is there still an opportunity for individuals to join this experiment?

"An examination of the clinicaltrials.gov website reveals that this trial is no longer recruiting patients, having last been updated on April 7th 2022. However, there are currently 183 other studies in need of volunteers."

Answered by AI

Are participants of this trial required to be over 25 years old?

"Prospective patients must between 18 and 40 years of age to be eligible for this trial. Alternatively, there are 43 studies designated for minors and 116 research programs catered to the elderly population."

Answered by AI

Could I become part of this medical research experiment?

"This study is seeking 451 individuals within the age range of 18-40 who have a history of maternal care between them. To qualify, applicants must possess access to both text messaging and the internet via smart phone or other device, be nulliparous pregnant women with singleton pregnancies in 27-37 weeks gestation, and meet the stipulated age criteria."

Answered by AI
~108 spots leftby Apr 2025