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OpenTrials
Completed

NCT Number: NCT01326169

ReDIAL: A Telephone Brief Intervention for Injured Emergency Department Patients

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rhode Island Hospital, Providence, Rhode Island, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Brief intervention

Behavioral

Telephone-delivered counseling

Standard Care

Behavioral

No intervention

Primary outcomes

  1. Change in number of patients with alcohol-related negative consequences from baseline to 4, 8, and 12 months post-randomization

    Time frame: 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 outcomes

  1. Evaluation of mechanisms of change model

    Time frame: 12 months post-randomization

    Determine the moderators and mediators of primary outcomes.

Sponsors and collaborators

Lead sponsor

Rhode Island Hospital

Other

Registry information

Acronym: ReDIAL

Important dates

Study start
2010
Primary completion
2013
Study completion
2014
First posted
Mar 30, 2011
Registry last updated
Sep 11, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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