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NCT01031615 · ClinicalTrials.gov registry record · Phase 1

Evaluation of the Child and Family Traumatic Stress Intervention

A Phase 1 study, sponsored by Yale University.

Completed
Registry status
Phase 1
Development phase
112
Enrollment target

NCT01031615: Completed Phase 1 study, sponsored by Yale University.

NCT01031615 is a Phase 1 study that has completed, run by Yale University. The registered enrollment target is 112 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01031615, a Phase 1 study, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 1
Development phase
112 participants
Enrollment target

Study Summary

The purpose of this study is to determine the efficacy of the Child and Family Traumatic Stress Intervention (CFTSI) in preventing the development of Posttraumatic Stress Disorder (PTSD) when implemented within 30 days of a potentially traumatic event.

Interventions

  • BEHAVIORAL Child and Family Traumatic Stress Interv (CFTSI)
  • BEHAVIORAL Psychoeducational Comparison

Trial Details

FieldValue
Enrollment Target 112 participants
Start Date 2005-10
Est. Completion 2009-09
Phase Phase 1
Yale University

1,492 total trials

What the finished NCT01031615 record still lists

NCT01031615 is an interventional study that assigns participants to a tested intervention. The registered 112 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% higher).

The record links to 0 conditions, and to 2 interventions - of which Child and Family Traumatic Stress Interv (CFTSI) is the first listed.

NCT01031615 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01031615 about?

NCT01031615 is a clinical study titled "Evaluation of the Child and Family Traumatic Stress Intervention". The purpose of this study is to determine the efficacy of the Child and Family Traumatic Stress Intervention (CFTSI) in preventing the development of Posttraumatic Stress Disorder (PTSD) when implemented within 30 days of a potentially traumatic event.

What is the current status of trial NCT01031615?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 112 participants. The study started on 2005-10. Estimated completion is 2009-09.

What interventions are being tested in trial NCT01031615?

The interventions under investigation include: Child and Family Traumatic Stress Interv (CFTSI) (BEHAVIORAL), Psychoeducational Comparison (BEHAVIORAL).

Who is sponsoring clinical trial NCT01031615?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01031615's enrollment target sits among peer trials

112 508th of 2000 higher than 1,489 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01031615, the US trial registry maintained by the National Library of Medicine. NCT01031615 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.