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Clinical Trials/NCT04535011
NCT04535011CompletedNot Applicable

PRACT: A Pragmatic Randomized Adaptive Clinical Trial to Investigate Controlling Alcohol Related Harms in a Low-Income Setting; Emergency Department Brief Interventions in Tanzania

Duke University1 site in 1 country674 target enrollmentStarted: October 12, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
674
Locations
1
Primary Endpoint
Change in number of binge drinking days (previous 4 weeks)

Study Overview

Brief Summary

Alcohol use is rapidly increasing in low- and middle-income countries, where it is inexpensive, readily available, poorly regulated, and there are few resources devoted to promoting safe alcohol use. A Brief Intervention based on a motivational interviewing framework has been shown to reduce alcohol use and alcohol-related harms. The investigators have translated and adapted a Brief Intervention for alcohol to the Tanzanian context and Swahili language called "Punguza Pombe Kwa Afya Yako (PPKAY)/ Reduce Alcohol for Your Health." This project will evaluate this intervention in injury patients presenting for care at the Kilimanjaro Christian Medical Center in Moshi, Tanzania. By using innovative adaptive clinical trial methods, the investigators will expedite the development of the most effective way to integrate this intervention into clinical care. By the end of this project, investigators will have identified the most effective brief intervention components and be able to characterize the intervention's effect overall. Additionally, investigators will standardize adaptive trial methods to revolutionize the science of clinical trials for behavioral sciences in low-resource settings.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Sequential
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •≥18 years of age)
  • •present seeking initial care at the KCMC ED for an acute (<24 hours) injury
  • •not clinically intoxicated (i.e., have capacity to consent).
  • •one or more of the following: 1) disclosed alcohol use prior to injury, 2) scored ≥8 on the AUDIT, 3) test positive (>0.0 g/dL) by alcohol breathalyzer.

Exclusion Criteria

  • •do not speak the native Swahili language
  • •too ill or unable to communicate
  • •prior enrollment in this study
  • •decline informed consent.

Arms & Interventions

Usual Care

No Intervention

No prevention or educational information verbally or written coinciding with current usual care

PPKAY

Experimental

One-time, 15-minute, nurse-led motivational interview discussing safe drinking behaviors, and negotiating change in alcohol use

Intervention: PPKAY (brief intervention) (Behavioral)

PPKAY with Standard Booster

Experimental

One-time, 15-minute, nurse-led motivational interview discussing safe drinking behaviors, and negotiating change in alcohol use.

Weekly standard text booster until final follow-up (e.g., "Reducing your alcohol intake to less than 4 drinks per day reduces your risk of alcohol-related consequences")

Intervention: PPKAY (brief intervention) (Behavioral)

PPKAY with Standard Booster

Experimental

One-time, 15-minute, nurse-led motivational interview discussing safe drinking behaviors, and negotiating change in alcohol use.

Weekly standard text booster until final follow-up (e.g., "Reducing your alcohol intake to less than 4 drinks per day reduces your risk of alcohol-related consequences")

Intervention: Standard Booster (Behavioral)

PPKAY with Personalized Booster

Experimental

One-time, 15-minute, nurse-led motivational interview discussing safe drinking behaviors, and negotiating change in alcohol use Weekly personalized text booster until final follow-up (e.g., "Remember to reduce your alcohol less than 4 drinks to achieve your goal of… [being a better husband].")

Intervention: PPKAY (brief intervention) (Behavioral)

PPKAY with Personalized Booster

Experimental

One-time, 15-minute, nurse-led motivational interview discussing safe drinking behaviors, and negotiating change in alcohol use Weekly personalized text booster until final follow-up (e.g., "Remember to reduce your alcohol less than 4 drinks to achieve your goal of… [being a better husband].")

Intervention: Personalized Booster (Behavioral)

Outcomes

Primary Outcomes

Change in number of binge drinking days (previous 4 weeks)

Time Frame: Baseline, 3 months, 6 months, 9 months, 12 months, 24 months

Secondary Outcomes

  • Change in quantity of alcohol use (previous 2 weeks)(Baseline, 3 months, 6 months, 9 months, 12 months, 24 months)
  • Change in depression(Baseline, 3 months, 6 months, 9 months, 12 months, 24 months)
  • Change in frequency of alcohol use (previous 2 weeks)(Baseline, 3 months, 6 months, 9 months, 12 months, 24 months)
  • Change in alcohol use disorder(Baseline, 3 months, 6 months, 9 months, 12 months, 24 months)
  • Change in alcohol-related harms measured by the Drinker Inventory of Consequences (DrInC)(Baseline, 3 months, 6 months, 9 months, 12 months, 24 months)

Investigators

Sponsor
Duke University
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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