Cognitive Behavioral Intervention to Reduce Procedural Anxiety Among Woman With High Risk Pregnancies With Scheduled Cesarean Deliveries
Status unconfirmed · Not applicable
Conditions studied: Procedural Anxiety, High Risk Pregnancy, Fetal Complications
In brief
The goals of this study are to determine the feasibility and efficacy of a brief, single-session cognitive-behavioral intervention for reducing preoperative and postoperative anxiety and for determining satisfaction with the delivery process in pregnant women scheduled for Cesarean delivery due to complications with their pregnancy. This will be done through a combination of psychoeducation and exposure therapy, where the participants will be walked through the steps of a Cesarean delivery in an operating room that mimics where the patient would actually be delivering. Follow-up will occur during the immediate and extended postpartum periods to determine satisfaction and levels of anxiety.
Key facts
- Study ID
- NCT04203082
- Run by
- University of Colorado, Denver
- People needed
- 50
- Starts
- 2020-07-23
- Expected to finish
- 2025-01-01
- Last updated by the study team
- 2024-02-22
Who can join
Age: 18 and older, up to 60. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Fetal Anomaly/Complication
- Planned Cesarean Delivery
You may not qualify if…
- Delivery planned at outside hospital
Where it is running
- Baylor College of Medicine — Houston, Texas, United States (enrolling)
- The University of Texas Health Science Center at Houston — Houston, Texas, United States (enrolling)
- Children's Hospital Colorado — Aurora, Colorado, United States (enrolling)
- Children's Mercy — Kansas City, Missouri, United States
Full record on ClinicalTrials.gov
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