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NCT03018132Active, not recruiting

Preeclampsia Research on Vitamin D, Inflammation, & Depression

The PROVIDE Study; Preeclampsia Research on Vitamin D, Inflammation, & Depression

Source: ClinicalTrials.gov · Last updated 21 Oct 2026

Brief summary (registry, in English)

This study is designed to comprehensively investigate the anti-inflammatory role of vitamin D in reproductive aged women, and its association with preeclampsia and depression. Findings will have substantial impact providing new information implicated in the development of preeclampsia (a condition that may include hypertension, tissue swelling caused by excessive fluid, and kidney stress) and postpartum depression (after birth). Additionally, the study is designed to understand how early mental health screening and evaluation can help pregnant women reduce their risk of developing postpartum depression. Testing the acceptability and effectiveness of this mental health screening, education and referral program at Cedars-Sinai Medical Center will provide valuable patient centered qualitative and quantitative data that can be used in future services planning. The study will enroll up to 200 pregnant women (in third trimester of pregnancy) in total.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
8 Dec 2016
Start date
1 Apr 2017
Primary completion date
1 Jul 2021
Lead sponsor
Cedars-Sinai Medical Center
NCT number
NCT03018132

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 1 Apr 2017 to the primary completion date, 1 Jul 2021
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Any diagnosis of psychosis, past or current (evident by either meds taken via medical intake, or in clinical assessment - SCID)
  • Current substance abuse (evident either via medical intake, or in clinical assessment - SCID)

Who the study is looking for

  • Female
  • Minimum 18 years of age
  • Patient at Cedars Sinai Medical Center, Los Angeles, CA
  • Between 20 and 40 weeks gestation (majority recruited at start of 3rd trimester between 26-32 weeks)
  • English or Spanish language preference

Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cedars-Sinai Medical Center
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.