Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01680614 · ClinicalTrials.gov registry record

The Efficacy of Computerized Alcohol Screening and Intervention (CASI) in At-Risk Emergency Department and Trauma Patients

A clinical trial, sponsored by University of California, Irvine.

Completed
Registry status
2,114
Enrollment target

NCT01680614: Completed study, sponsored by University of California, Irvine.

NCT01680614 is a clinical trial that has completed, run by University of California, Irvine. The registered enrollment target is 2,114 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01680614 has completed, sponsored by University of California, Irvine.

COMPLETED
Registry status
2,114 participants
Enrollment target

Study Summary

The purpose of this research is to examine the effectiveness of computerized alcohol screening and brief intervention in the UC Irvine Medical Center Emergency Department (ED) and Trauma Patients. Brief interventions have a high potential impact in ED and Trauma populations. Computerized alcohol screening and brief intervention (CASI) is a fast and easy to use tool for patients and healthcare providers. CASI mitigates barriers to proper screening and intervention, including time, availability of trained personnel, patient comfort, and language barriers. CASI provides the Alcohol Use Disorders Identification Test (AUDIT) followed by a brief intervention and customized alcohol intake recomendations for the patient. The intervention of this study will be the addition of a brief CASI questionnaire to the standard of care for a random subset of subjects. All subjects who screen positive for hazardous alcohol use will be followed up and reassessed for alcohol use. The researchers hypothesize that the addition of CASI will lead to a decrease in alcohol intake within three months. The basis of this research is evidence of the effectiveness in the CASI system, the growing public health issue of alcohol abuse, the need to be able to provide effective screening and brief intervention in the high volume ED settings, and findings that the primary method to reduce traumatic death is prevention.

Interventions

  • BEHAVIORAL CASI

Trial Details

FieldValue
Enrollment Target 2,114 participants
Start Date 2013-01-01
Est. Completion 2015-06-29
University of California, Irvine

368 total trials

What the finished NCT01680614 record still lists

NCT01680614 is an observational study that tracks outcomes without assigning an intervention. Its 2,114 participants enrollment target places it among the larger protocols in the corpus.

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

NCT01680614 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01680614 about?

NCT01680614 is a clinical study titled "The Efficacy of Computerized Alcohol Screening and Intervention (CASI) in At-Risk Emergency Department and Trauma Patients". The purpose of this research is to examine the effectiveness of computerized alcohol screening and brief intervention in the UC Irvine Medical Center Emergency Department (ED) and Trauma Patients. Brief interventions have a high potential impact in ED and Trauma populations. Computerized alcohol scr...

What is the current status of trial NCT01680614?

This trial is currently completed. The enrollment target is 2,114 participants. The study started on 2013-01-01. Estimated completion is 2015-06-29.

What interventions are being tested in trial NCT01680614?

The interventions under investigation include: CASI (BEHAVIORAL).

Who is sponsoring clinical trial NCT01680614?

This trial is sponsored by University of California, Irvine, which has 368 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05916430 · 2,120 participants

    Screening for Autism in 9-Month-Olds by Measuring Social Visual Engagement

  • NCT05967273 · 2,106 participants · NA

    CirrhosisRx CDS System

  • NCT05681624 · 2,124 participants · NA

    Maternal Oxygen Supplementation for Intrauterine Resuscitation

  • NCT04649242 · 2,100 participants · Phase 3

    Randomized Study in Children and Adolescents With Migraine: Acute Treatment

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01680614, the US trial registry maintained by the National Library of Medicine. NCT01680614 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.