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NCT02465177 Clinical Trial

Tailoring Screening, Brief Intervention, and Referral to Treatment for Medical ICU Survivors

Alcohol Use Disorders Clinical Trial

Official title:
Tailoring Screening, Brief Intervention, and Referral to Treatment for Medical Intensive Care Unit Survivors

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02465177
Other study ID # 13-3159
Secondary ID UL1TR001082
Status Recruiting
Phase
First received
Last updated
Start date July 2014
Est. completion date December 2021

Study information
Verified date February 2021
Source University of Colorado, Denver
Contact Diandra Reed, BS
Phone 3037246079
Email kathryne.reed@ucdenver.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Unhealthy alcohol use is present in up to 38% of the 4 million patients admitted to an American intensive care unit (ICU) each year in the US. Despite the high prevalence of unhealthy alcohol use in ICU survivors, routine interventions targeted at reducing alcohol consumption, alcohol-related consequences, and illness related to alcohol are not currently part of the multidisciplinary approach to critical care. Although screening, brief intervention, and referral to treatment (SBIRT) has been described in several healthcare settings, it fails to address common characteristics of medical ICU survivors including high rates of alcohol use disorders, cognitive dysfunction, psychiatric comorbidities, and intimate involvement of friends and family. This study uses a qualitative approach to further understand the needs of medical ICU survivors with unhealthy alcohol use. The investigators hypothesize that there are common, modifiable barriers to improving alcohol-related outcomes

Recruitment information / eligibility
Status Recruiting
Enrollment 28
Est. completion date December 2021
Est. primary completion date November 2021
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - 18 years or older - admitted to the medical ICU - resolution of critical illness - resolution of delirium/agitation - AUDIT score 8 or greater for men, 5 or greater for women Exclusion Criteria: - unable to provide informed consent - prisoner - Unable to speak or write in English - Pregnant

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of Colorado Hospital Aurora Colorado

Sponsors (1)
Lead Sponsor Collaborator
University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in alcohol use Change in alcohol use as assessed using a Semi-structured qualitative interview 3 months
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