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Journal Article

Citation

Spirito A, Sindelar-Manning H, Colby SM, Barnett NP, Lewander W, Rohsenow DJ, Monti PM. Arch. Pediatr. Adolesc. Med. 2011; 165(3): 269-274.

Affiliation

Brown University Center for Alcohol and Addiction Studies, University Box G-S121-4, Providence, RI 02912. Anthony_Spirito@brown.edu.

Copyright

(Copyright © 2011, American Medical Association)

DOI

10.1001/archpediatrics.2010.296

PMID

21383276

Abstract

OBJECTIVE: To determine whether a brief individual motivational interview (IMI) plus a family motivational interview (Family Check-Up [FCU]) would reduce alcohol use in adolescents treated in an emergency department after an alcohol-related event more effectively than would an IMI only. DESIGN: Two-group randomized design with 3 follow-up time points. SETTING: An urban regional level I trauma center. PARTICIPANTS: Adolescents aged 13 to 17 years (N = 125) with a positive blood alcohol concentration as tested using blood, breath, or saliva. INTERVENTIONS: Either IMI or IMI plus FCU. MAIN OUTCOME MEASURES: Drinking frequency (days per month), quantity (drinks per occasion), and frequency of high-volume drinking (≥5 drinks per occasion). RESULTS: Both conditions resulted in a reduction in all drinking outcomes at all follow-up points (P < .001 for all), with the strongest effects at 3 and 6 months. Adding the FCU to the IMI resulted in a somewhat better outcome than did the IMI only on high-volume drinking days at 3-month follow-up (14.6% vs 32.1%, P = .048; odds ratio, 2.76; 95% confidence interval, 0.99-7.75). CONCLUSIONS: Motivational interventions have a positive effect on drinking outcomes in the short term after an alcohol-related emergency department visit. Adding the FCU to an IMI resulted in somewhat better effects on high-volume drinking at short-term follow-up than did an IMI only. The cost of extra sessions necessary to complete the FCU should be weighed against the potential benefit of reducing high-volume drinking when considering adding the FCU to an IMI for this population. Trial Registration  clinicaltrials.gov Identifier: NCT 00247221.


Language: en

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