Multilevel Community-Centered Intervention to Reduce Pregnancy Related and Associated Morbidity and Mortality (PRAMM) Disparities
Recruiting
N/A
Interventional Study
Provider Confidence
Provider Behavior
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 480 (estimated)
- Sponsor
- Michigan State University · Other
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About This Trial
The goal of the study involving human subjects is to train providers to address patient-provider interactions. The study will survey providers to assess pre-post knowledge, understanding, and behavior changes.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Providing care to pregnant and postpartum women in Wayne, Kent, and Genesee Counties in MI
Exclusion Criteria:
* None
Contacts