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Preventing Drug Abuse Among Hispanic Adolescents

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Columbia University

Status

Completed

Conditions

Drug Abuse

Treatments

Behavioral: Prevention Program

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02375516
R01DA031477 (U.S. NIH Grant/Contract)
AAAK6105

Details and patient eligibility

About

The planned research aims to delay the onset of drug use and reduce harmful use and abuse among Hispanic youths. The culturally-tailored prevention program will be delivered to youths by computer. Over 5 years, the program will be developed and tested in a randomized clinical trial. The intervention program will include 10 initial sessions, followed by annual booster sessions. Outcome measurements will involve baseline, post-intervention, and three annual follow-up data collections.

The study's primary hypothesis is that rates of 30-day alcohol and drug use will be lower among participants assigned to receive the intervention. If proven to be efficacious, the program will be revised and disseminated nationally.

Full description

America's largest ethnic minority group, Hispanics are also a youthful population: one-third of Hispanic Americans are less than 18 years old. Unfortunately, young Hispanic Americans are an at-risk population more likely than their majority culture peers to drop out of school, become involved in the criminal justice system, fall prey to violence, and face lifelong economic problems. Hispanic youths are also at risk for early drug use and subsequent harmful use and abuse. As early as eighth grade and relative to their Black and White peers, Hispanic adolescents report higher rates of most harmful substances. Drug use continues to pose problems for Hispanic youths throughout adolescence and into adulthood.

Enrollment

678 patients

Sex

All

Ages

12 to 15 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 12 to 15 years old
  • Hispanic ethnicity

Exclusion criteria

  • None

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

678 participants in 2 patient groups

Prevention Program
Experimental group
Description:
Youths in the intervention-arm will interact online with the initial intervention program between pretest and posttest measurement occasions and will interact with booster sessions subsequent to 1- and 2-year follow-up measurement occasions.
Treatment:
Behavioral: Prevention Program
Control group
No Intervention group
Description:
Youths assigned to the control arm will receive no intervention.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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