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Enhanced Doula Support for Pregnancy and Mental Health

Deconstructing Maternal Burdens: Doulas and the Community Unite for Health

Recruiting N/A Interventional Study
Pregnancy Post Partum Doula Care Postpartum Depression (PPD) Perinatal Depression Perinatal Anxiety Health Disparities Pregnancy Complications Maternal Adverse Outcomes
More trials: Depression clinical trials· Depression trials in Florida
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
15 – 49
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
516 (estimated)
Sponsor
University of Florida · Other
Who this trial is looking for

This trial is looking for pregnant individuals enrolled in Medicaid. Participants will receive either enhanced doula support or standard doula care during and after pregnancy to see which is more helpful for mental health.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am 15-49 years old
  • I am 14-28 weeks pregnant
  • I am eligible for Medicaid
  • I live in North Central Florida

You may not be able to join if

  • I have severe physical health conditions that interfere with participation
  • I have severe mental health conditions that interfere with participation

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial
This study is a randomized controlled trial comparing two models of doula support for pregnant individuals enrolled in Medicaid: an enhanced doula support model, in which support starts earlier in pregnancy, occurs more frequently, and continues through the first year after birth, versus the standard doula care currently covered by Medicaid in Florida. The study also builds the doula workforce ne…
Trial Locations

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Eligibility Criteria
Inclusion Criteria: * 15-49 years old * 14-28 weeks pregnant * Medicaid Eligible * Resides in North Central Florida Exclusion Criteria: * Severe physical or mental health conditions that Interfere with participation
Contacts

No contact information available.

NCT ID: NCT07799805 Source: ClinicalTrials.gov