Alcohol Drinking Clinical Trial
— ReDIALOfficial title:
ReDIAL: A Telephone Brief Intervention for Injured Emergency Department Patients
Verified date | September 2014 |
Source | Rhode Island Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The goal of this study is to reduce impaired driving, risky driving and alcohol-related negative consequences among injured emergency department (ED) patients through a telephone brief intervention. This study will allow researchers to test a novel method of brief intervention that has the potential to be convenient and efficient mechanism to deliver an intervention to an at-risk population. Eligible patients will be consented in the ED, will receive an assessment and then will be randomized into one of two conditions: 1) telephone brief intervention or 2) a comparison control group with a home safety educational program. The participant will also receive an appointment for an initial telephone call. Both conditions will be provided over three telephone sessions: the initial call (immediately following randomization) and two booster calls at 2 weeks and 6 weeks after randomization. Participants will provide information about their alcohol use, alcohol-related injuries, impaired driving, and other driving related negative consequences at 4, 8, and 12 months post-randomization.
Status | Completed |
Enrollment | 730 |
Est. completion date | May 2014 |
Est. primary completion date | March 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - English or Spanish speaking - Age greater than 17 years - ASSIST score >=11 - Injured Emergency Department patient at time of consent Exclusion Criteria: - Medically unable to give consent - Not English or Spanish speaking - Homeless - Cannot be contacted by telephone |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Rhode Island Hospital | Providence | Rhode Island |
United States | The Miriam Hospital | Providence | Rhode Island |
Lead Sponsor | Collaborator |
---|---|
Rhode Island Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in number of patients with alcohol-related negative consequences from baseline to 4, 8, and 12 months post-randomization | Specifically, the effect of the intervention on alcohol-related injuries and alcohol-related psychosocial consequences from baseline at 4, 8, and 12 months post-randomization. | Change from baseline in alcohol-related negatve consequences at 4, 8, and 12 months | No |
Secondary | Evaluation of mechanisms of change model | Determine the moderators and mediators of primary outcomes. | 12 months post-randomization | No |
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