Worcester, MANCT05884190Now EnrollingIRB Ready

Postpartum Hypertension Clinical Trial in Worcester, MA

Access cutting-edge postpartum hypertension treatment through this clinical trial at a research site in Worcester. Study-provided care at no cost to qualified participants.

Sponsored by Yale University

Quick Self-Assessment

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Expert Care in Worcester

Access postpartum hypertension specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related postpartum hypertension treatment provided free

Apply for This Worcester Location

Check if you qualify for this postpartum hypertension clinical trial in Worcester, MA

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Worcester

    Convenient for MA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Worcester site if eligible
  4. 4Begin participation

About This Postpartum Hypertension Study in Worcester

The investigators primary project goal is to improve clinical outcomes, including mental health outcomes, among postpartum at-risk women experiencing health disparities by increasing awareness, detection, and timely care of postpartum hypertension, mental health and cardiovascular complications. The investigators will accomplish this by comparing the effectiveness of two multi-component multi-level healthcare delivery models focused on early detection and control of postpartum hypertension and the social and mental health factors known to impact maternal outcomes, with the current standard of care and with each other.

Sponsor: Yale University

Who Can Participate

Inclusion Criteria

Delivery of singleton live birth (twins reduced to singleton or with vanishing twin syndrome prior to 14 weeks qualify)
English or Spanish speaking
Viable pregnancy 24 weeks of gestation or above (Child can be in NICU to participate)
Medicaid or the equivalent within each state (for example, Connecticut has Husky insurance) or uninsured
Must living in one of the three states involved in this study (Connecticut, Massachusetts, New York) and preferably within the geographical area of each of the hospitals

Exclusion Criteria

Multifetal pregnancy (since are they at increased risk for key outcomes)
Gestational age \<24 weeks;
Known major fetal anomaly in current pregnancy or stillbirth
Actively using illicit/illegal substances (such as cocaine, heroin and other types of illicit opiates such as fentanyl) as noted in delivery hospitalization notes
Active suicidal ideation with intent and plan
Known primary psychotic disorder (i.e. schizophrenia, or schizoaffective disorder)
Plans to move out of the state within 6 months
Incapable of consent
Severe medical complications that don't allow a mother to do the study effectively (for example, active treatment for cancer, dialysis etc. )
Physician or provider refusal
Patient refusal
Incarcerated or institutionalized
Stillbirth Births that result in the newborn being under the care of another person or institution other than the birthing individual (e.g. adoption, state involvement) will be evaluated on an individual basis to determine if that person should be included. For participants without access to a phone, we will explore if there are options that will allow them to have access to a devise for the times when they need to communicate with the study team. If not, they will not be able to participate in the study since this study requires phone or telehealth communication with research staff and/or APPs, and CHWs depending on study phase.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Worcester?

Yes, this clinical trial (NCT05884190) has an active research site in Worcester, MA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Postpartum Hypertension Treatment Options in Worcester, MA

If you're searching for postpartum hypertension treatment options in Worcester, MA, this clinical trial (NCT05884190) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Worcester research site is actively enrolling participants for this clinical trial. You'll receive care from experienced postpartum hypertension specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all postpartum hypertension clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Worcester, MA