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NCT02615717 · ClinicalTrials.gov registry record · NA

Using Attentional Bias Modification to Address Trauma Symptoms

A NA study of Posttraumatic Stress Disorder, sponsored by University of Nebraska Lincoln.

Completed
Registry status
NA
Development phase
6
Enrollment target
1
Study location

NCT02615717 is a NA study of Posttraumatic Stress Disorder that has completed, run by University of Nebraska Lincoln. The registered enrollment target is 6 participants, below the 112-participant average among 117 other Posttraumatic Stress Disorder trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02615717, a NA study of Posttraumatic Stress Disorder, has completed, sponsored by University of Nebraska Lincoln.

COMPLETED
Registry status
NA
Development phase
6 participants
Enrollment target
1
Study location

Study Summary

Threat-related attentional biases have been identified as a possible precursor to the onset and maintenance of posttraumatic stress disorder (PTSD). As a result, protocols such as Attention Bias Modification (ABM) have been developed and utilized to treat these attentional biases in adults diagnosed with PTSD. However, to-date, ABM protocols have not been examined for use specifically among victims of sexual assaults. Participants are 20 undergraduate women enrolled in a Midwest university. The efficacy of ABM in this population will be assessed, as will the relationship between ABM and PTSD symptom clusters and outcome variables such as anxiety and depression scores.

Interventions

  • BEHAVIORAL Attention Bias Modification

Study Locations (1)

Nebraska

  • University of Nebraska-Lincoln - Lincoln

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2015-11
Est. Completion 2016-04
Phase NA

Sponsor

University of Nebraska Lincoln

24 total trials

What the Registry Record Tells You About NCT02615717

The ClinicalTrials.gov registry entry for NCT02615717 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 112-participant average among 117 other Posttraumatic Stress Disorder trials with a reported enrollment target (95% lower). The listed sponsor is University of Nebraska Lincoln, which has 24 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Posttraumatic Stress Disorder appearing as the primary indexed condition, and to 1 intervention - of which Attention Bias Modification is the first listed.

NCT02615717 reports 1 study location spanning 1 distinct geographic area - top geographies include Nebraska.

Frequently Asked Questions

What is clinical trial NCT02615717 about?

NCT02615717 is a clinical study titled "Using Attentional Bias Modification to Address Trauma Symptoms". Threat-related attentional biases have been identified as a possible precursor to the onset and maintenance of posttraumatic stress disorder (PTSD). As a result, protocols such as Attention Bias Modification (ABM) have been developed and utilized to treat these attentional biases in adults diagnosed...

What is the current status of trial NCT02615717?

This trial is currently completed. It is a NA study. The enrollment target is 6 participants. The study started on 2015-11. Estimated completion is 2016-04.

What conditions does trial NCT02615717 study?

This clinical trial studies the following conditions: Posttraumatic Stress Disorder.

What interventions are being tested in trial NCT02615717?

The interventions under investigation include: Attention Bias Modification (BEHAVIORAL).

Who is sponsoring clinical trial NCT02615717?

This trial is sponsored by University of Nebraska Lincoln, which has 24 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02615717 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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, or report a data error.