ReDIAL: A Telephone Brief Intervention for Injured Emergency Department Patients

Not Applicable

Completed

• Conditions: Alcohol Drinking

• Registration Number: NCT01326169
• Lead Sponsor: Rhode Island Hospital

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-03
• Study First Submitted: 2011-03-28
• Study First Submitted QC: 2011-03-29
• Study First Posted: 2011-03-30
• Primary Completion: 2013-03
• Study Completion: 2014-05
• Status Verified: 2014-09
• Last Update Submitted: 2014-09-10
• Last Update Posted: 2014-09-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 730

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in number of patients with alcohol-related negative consequences from baseline to 4, 8, and 12 months post-randomization	Change from baseline in alcohol-related negatve consequences at 4, 8, and 12 months	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.

Secondary Outcome Measures

Name	Time	Method
Evaluation of mechanisms of change model	12 months post-randomization	Determine the moderators and mediators of primary outcomes.

Trial Locations

Locations (2)

Rhode Island Hospital; 🇺🇸 Providence, Rhode Island, United States

The Miriam Hospital; 🇺🇸 Providence, Rhode Island, United States