Preventing Mood and Anxiety Problems After Cesarean Delivery
Official title: Preventing Maternal Mood, Anxiety, and Trauma Symptoms after Cesarean Delivery
Funded at University of Colorado Denver · NIH-11394478 · Data updated 2026-11-12
A low-cost, one-hour intervention given to pregnant patients having a cesarean delivery to help reduce mood, anxiety, and trauma symptoms later on.
Quick facts
| Grant type | NIH-funded research |
|---|---|
| Study type | NIH-funded research |
| Funding institution | University of Colorado Denver NIH-funded |
| Lab location | 1 site (Aurora, UNITED STATES) |
| Project start | May 3, 2024 |
| Project end | April 30, 2027 |
| Funding year | 2026 |
| Award (this year) | $189,000 |
| NIH project number | 5R34MH133685-03 |
| Project ID | NIH-11394478 on NIH RePORTER |
Who could benefit from this research
✓Could help
Pregnant individuals at high risk for PMATS who are planning a cesarean delivery and are open to a one-session preventive intervention.
✕Less likely to help
Individuals not undergoing cesarean delivery or those who do not experience PMATS risk factors may derive little or no benefit.
What this research studies
This project plans to offer a brief, single-session cognitive-behavioral approach designed for high-risk pregnancies requiring cesarean delivery. It builds on prior work showing that a one-hour program can lessen anxiety sensitivity and traumatic stress around surgery. The intervention includes psychoeducation and a controlled exposure to the operating room experience, aiming to prevent PMATS before they start. The study will be conducted with pregnant patients at risk for PMATS, with the goal of making mental health support more accessible and affordable.
Why it matters
Potential benefit: If successful, the program could reduce the risk of mood and anxiety disorders after cesarean delivery for mothers and improve overall perinatal well-being.
How similar studies have gone: Previous small studies suggest single-session interventions can reduce anxiety-related symptoms around surgical events, but larger trials are needed for conclusive evidence.
Where this research is happening
-
University of Colorado Denver
Aurora, United States Active
Researchers
- Principal investigator: Wood, Cristina L — University of Colorado Denver
- Study coordinator: Wood, Cristina L
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About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.