Stress Phenotypes and Preterm Birth
Columbia University · with National Institute on Minority Health and Health Disparities (NIMHD) · NCT05229666
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 200
- US sites recruiting
- 1
- Study start
- December 9, 2021
- Record last updated
- May 14, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Pregnancy ends in preterm birth (PTB) for approximately 1 in 10 women, though more often for Non-Hispanic Black women, 14.12% PTB rate, compared to 9.09% for Non-Hispanic White women. Psychosocial stress and childhood trauma each are associated with risk for PTB and PTB has an intergenerational impact: mothers born preterm are more likely to give birth preterm, especially amongst Black women. In this project, we will study mitochondria, which contain their own genome, the mitochondria DNA, and are inherited from the mother, as they represent a potential intersection point between psychosocial experiences and their biological embedding in underlying disease outcomes such as PTB
Being studied: Cognitive Challenge
Conditions: Preterm Birth; Inflammation; Stress; Mental Health Issue
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Pregnant women 18 years of age or older (based on self-report)
- Not currently smoking, drinking alcohol, or taking drugs (based on self-report)
- Planning to deliver at CUIMC/NYP (based on self-report)
- In the first or second trimester of pregnancy (prior to 28 weeks gestation) (based on self-report of estimated date of delivery)
Exclusion Criteria
- Multi-fetal pregnancy (based on self-report)
- Taking medications regularly that affect the cardiovascular and inflammatory systems, including NSAIDS and other anti-inflammatories, α blockers, β blockers, corticosteroids, chronic-use asthma medications (e.g. beta2- adrenoceptor agonists) (based on self-report)
- This does NOT include baby aspirin or low-dose aspirin, as baby aspirin / low-dose aspirin is not normally considered to be an NSAID.
- Inflammatory conditions including rheumatoid arthritis, lupus, and multiple sclerosis (based on self-report)
Recruiting US locations
Columbia University Irving Medical Center
New York, NY 10032
Site contact: Catherine Monk, PhD · 917-543-6031 · cem31@columbia.edu
Study contacts (from the official record)
- Catherine Monk, PhD · 646-774-8941 · cem31@cumc.columbia.edu
- Elizabeth Werner, PhD · 646-774-8835 · ew150@cumc.columbia.edu
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