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Not yet recruiting NCT07657221

Impact of Risk Feedback on Behavioral Trajectories

No phase Interventional Healthy Alcohol Consumption

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: PHEN feedback, PHEN+GENE Feedback, Control.
Who it may be relevant to
Registry conditions: Healthy, Alcohol Consumption. Basic parameters: 17 years — 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Alcohol Metabolism and Disease Risk in Asians: Examining the Impact of Personalized Phenotypic/Genotypic Feedback on Early Drinking Trajectories

Overview

The goal of this study is to examine the effects of providing personalized information about behavioral, physical, and genetic factors that are associated with elevations in risk for some health problems. The main research question is: can we affect young adult behaviors through communication about these health-related risks? Participants will be asked to complete an in-person baseline session where they provide a DNA sample, complete online surveys, and do a brief interview. They will then receive one of several brief online information sessions and be followed in online surveys approximately every 3 months over the next 2 years.

Interventions

  • Behavioral PHEN feedback
    Feedback on alcohol response (phenotype)
  • Genetic PHEN+GENE Feedback
    Feedback on both phenotype and genotype (PHEN+GENE)
  • Other Control
    Feedback that serves as control

Primary outcome measures

  • Drinking frequency [Time frame: up to 2 years post-intervention]
  • Average alcohol quantity [Time frame: up to 2 years post-intervention]
Secondary outcome measures (4)
  • Amount of alcohol consumed [Time frame: up to 2 years post-intervention]
  • Maximum daily alcohol [Time frame: up to 2 years post-intervention]
  • Use of flush cures [Time frame: up to 2 years post-intervention]
  • Use of drinking behavioral strategies [Time frame: up to 2 years post-intervention]

Eligibility criteria

Inclusion criteria

  • USC student of Chinese, Japanese, Korean, or Vietnamese heritage

Exclusion criteria

  • not a USC student, not 17-25 years old, not of Chinese, Japanese, Korean, or Vietnamese heritage

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

United States · 1 center
  • University of Southern California — Los Angeles

Identifiers

NCT: NCT07657221 · UP-24-00754 · R01AA032036

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗