- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02465177
Tailoring Screening, Brief Intervention, and Referral to Treatment for Medical ICU Survivors
February 17, 2021 updated by: University of Colorado, Denver
Tailoring Screening, Brief Intervention, and Referral to Treatment for Medical Intensive Care Unit Survivors
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
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
28
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Colorado
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Aurora, Colorado, United States, 80045
- Recruiting
- University of Colorado Hospital
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Contact:
- Diandra Reed, BS
- Phone Number: 303-724-6079
- Email: kathryne.reed@ucdenver.edu
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 100 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Patients admitted to one of 3 medical intensive care units in the Denver metropolitan area
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in alcohol use
Time Frame: 3 months
|
Change in alcohol use as assessed using a Semi-structured qualitative interview
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2014
Primary Completion (Anticipated)
November 1, 2021
Study Completion (Anticipated)
December 1, 2021
Study Registration Dates
First Submitted
May 26, 2015
First Submitted That Met QC Criteria
June 3, 2015
First Posted (Estimate)
June 8, 2015
Study Record Updates
Last Update Posted (Actual)
February 18, 2021
Last Update Submitted That Met QC Criteria
February 17, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 13-3159
- UL1TR001082 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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