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NCT01307293 · ClinicalTrials.gov registry record · NA

Prevention of Postpartum Traumatic Stress (PTSD) in Mothers With Preterm Infants.

A NA study, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
110
Enrollment target

NCT01307293: Completed NA study, sponsored by Stanford University.

NCT01307293 is a NA study that has completed, run by Stanford University. The registered enrollment target is 110 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01307293, a NA study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
110 participants
Enrollment target

Study Summary

The purpose of the study includes: 1. To develop a treatment manual and pilot test this treatment intervention which is designed to prevent and reduce psychological distress in parents who have infants hospitalized in the neonatal intensive care unit (NICU). 2. To conduct a treatment intervention study in which parents of NICU infants will receive a 6-12 session treatment designed to reduce psychological distress, and to compare outcomes with parents who do not receive the intervention. We hope to learn whether or not a simple psychotherapeutic and psychoeducational intervention offered to parents of NICU infants can prevent or minimize the development of symptoms of psychological distress in parents, including symptoms of anxiety and depression and posttraumatic stress disorder (PTSD).

Interventions

  • BEHAVIORAL Cognitive behavior therapy

Trial Details

FieldValue
Enrollment Target 110 participants
Start Date 2011-04
Est. Completion 2014-06
Phase NA

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT01307293

The ClinicalTrials.gov registry entry for NCT01307293 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Cognitive behavior therapy is the first listed.

NCT01307293 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01307293 about?

NCT01307293 is a clinical study titled "Prevention of Postpartum Traumatic Stress (PTSD) in Mothers With Preterm Infants.". The purpose of the study includes: 1. To develop a treatment manual and pilot test this treatment intervention which is designed to prevent and reduce psychological distress in parents who have infants hospitalized in the neonatal intensive care unit (NICU). 2. To conduct a treatment intervention s...

What is the current status of trial NCT01307293?

This trial is currently completed. It is a NA study. The enrollment target is 110 participants. The study started on 2011-04. Estimated completion is 2014-06.

What interventions are being tested in trial NCT01307293?

The interventions under investigation include: Cognitive behavior therapy (BEHAVIORAL).

Who is sponsoring clinical trial NCT01307293?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.