Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
985

Summary

Conditions
  • Alcohol Use Disorder
  • Injury Traumatic
  • Trauma
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Sequential AssignmentIntervention Model Description: Study Phase 1: The investigators will evaluate whether PPKAY with personalized text booster or PPKAY with standard text booster will reduce the quantity or frequency of alcohol use, the number of binge drinking events or the number of alcohol-related consequences based on the Drinker Inventory of Consequences (DrInC) compared to usual care. Study Phase 2: The investigators will evaluate whether a standard or personalized text booster is an inferior supplement to PPKAY. Study Phase 3: The investigators will evaluate if PPKAY alone is more or less effective compared to the superior arm from Study Phase 2 (PPKAY with personalized text booster or PPKAY with standard text booster).Masking: Double (Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04535011
Collaborators
Kilimanjaro Christian Medical Centre, Tanzania
Investigators
Principal Investigator: Catherine A Staton, MD Duke University