Depression Clinical Trial
— PROVIDEOfficial title:
The PROVIDE Study; Preeclampsia Research on Vitamin D, Inflammation, & Depression
Verified date | February 2024 |
Source | Cedars-Sinai Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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 | Active, not recruiting |
Enrollment | 200 |
Est. completion date | July 2025 |
Est. primary completion date | July 1, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 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 Exclusion Criteria: - 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) |
Country | Name | City | State |
---|---|---|---|
United States | Cedars-Sinai Medical Center | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
Cedars-Sinai Medical Center | Maternal Mental Health NOW |
United States,
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* Note: There are 56 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Depressive symptoms | as measured by reliable and validated screening tool (EPDS) | 5 months | |
Primary | Depression Diagnosis | as measured by diagnostic interview (SCID) | 5 months | |
Secondary | Anxiety symptoms | as measured by the OASIS | 5 months | |
Secondary | Post-traumatic stress symptoms | as measured by the IES | 5 months | |
Secondary | Perceived stress | as measured by the PSS | 5 months | |
Secondary | Acceptability of Mental Health Program | Results will be based on data from structured (Likert-scale) surveys completed at 4 time points, from the patient perspective | 5 months | |
Secondary | Benefits of Mental Health Program | Results will be based on data from the follow-up structured (Likert-scale) survey | 5 months | |
Secondary | Feasibility of Mental Health Program | The program's feasibility and MMH-Now training will be rated by clinic staff according to structured surveys completed at multiple time points, e.g. pre/post training. | 5 months | |
Secondary | Inflammation_IL6 | as measured by serum Interleukin-6 | 5 months | |
Secondary | Inflammation_CRP | as measured by serum hs_CRP | 5 months | |
Secondary | Vitamin D deficiency | as measured by serum 25(OH)D levels | 5 months |
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