LAC+USC Medicine Center Emergency Department
Los Angeles, California, 90033, United States
NCT Number: NCT02158949
In this study, the investigators will be developing and testing a mobile phone text message intervention to reduce alcohol use for people at risk of alcohol dependence. The investigators hypothesize that this intervention will be acceptable to participants, and that they will stay in the intervention until it's one week completion.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Los Angeles, California, 90033, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 1 week
percentage of patients that do not opt out of messages prior to 1 week completion
Time frame: 1 month
Feasibility of follow up of urban low-income at risk drinkers by phone defined as number of patients can be contacted at one months to complete assessment of alcohol use
Time frame: 1 month
patients reported number of days drinking any alcohol in prior 30 days, baseline report minus 1 month follow up report
Time frame: 1 month
patients reported number of heavy drinking days in prior 30 days (3 or more standard sized drinks per episode for women and 4 or more standard sized drinks per episode for men), baseline report minus 1 month follow up report
Time frame: 1 month
Participants reported desire to change via the Change Questionnaire applied to risky alcohol use.[1] The Change questionnaire has a Cronbach's alpha of 0.86 when applied to alcohol use.[2] Minimum score is 0 (low motivation to change) to maximum 120 (high motivation to change).
University of Southern California
Other
Mobilizing to Reduce Overuse of Alcohol in Emergency Department Patients
Acronym: mROAD
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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