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NCT07684521 · ClinicalTrials.gov registry record · NA
Debriefing Consult for Psychiatric Symptoms After Severe Maternal Morbidity
A NA study, sponsored by Cedars-Sinai Medical Center.
- Not yet
- Registry status
- NA
- Development phase
- 52
- Enrollment target
NCT07684521 is a NA study that has not yet begun recruiting, run by Cedars-Sinai Medical Center. The registered enrollment target is 52 participants.
The verdict
NCT07684521, a NA study, has not yet begun recruiting, sponsored by Cedars-Sinai Medical Center.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 52 participants
- Enrollment target
Study Summary
The primary objective of this study is to determine if a maternal fetal medicine (MFM) debriefing consult six to eight weeks postpartum reduces self-reported post-traumatic stress, depression, and anxiety symptoms following a delivery complicated by severe maternal morbidity (SMM). Individuals with a delivery complicated an intensive care unit (ICU) admission and/or blood product transfusion \>4 units will be included in this study. Participants will be randomized to an intervention or control group; all participants will complete patient questionnaires that screen for post-traumatic stress disorder, depression, and anxiety. Those in the control group will receive a virtual MFM debriefing consult at six weeks postpartum and those in the intervention group will have the option for a consult at twelve weeks postpartum, after the completion of the questionnaires.
Interventions
- BEHAVIORAL Virtual maternal fetal medicine debriefing consult
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2026-07-01 |
| Est. Completion | 2030-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07684521
The ClinicalTrials.gov registry entry for NCT07684521 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cedars-Sinai Medical Center, which has 339 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Virtual maternal fetal medicine debriefing consult is the first listed.
NCT07684521 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07684521 about?
NCT07684521 is a clinical study titled "Debriefing Consult for Psychiatric Symptoms After Severe Maternal Morbidity". The primary objective of this study is to determine if a maternal fetal medicine (MFM) debriefing consult six to eight weeks postpartum reduces self-reported post-traumatic stress, depression, and anxiety symptoms following a delivery complicated by severe maternal morbidity (SMM). Individuals with ...
What is the current status of trial NCT07684521?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 52 participants. The study started on 2026-07-01. Estimated completion is 2030-07.
What interventions are being tested in trial NCT07684521?
The interventions under investigation include: Virtual maternal fetal medicine debriefing consult (BEHAVIORAL).
Who is sponsoring clinical trial NCT07684521?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
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