NCT04579068

Brief Summary

Problematic alcohol use can lead to worse social and health related consequences for underserved minorities, requiring urgent intervention. By training underserved minority health professional students, this proposed project will develop and test the feasibility of an innovative and culturally tailored intervention for adults studying at a minority institution, with specific focus on alcohol screening, brief intervention, and referral of treatment (SBIRT). This proposal is expected to have a positive impact on alcohol reduction and prevention for minority communities

Trial Health

45
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
6mo left

Started Aug 2021

Longer than P75 for not_applicable

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress91%
Aug 2021Oct 2026

First Submitted

Initial submission to the registry

October 1, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 8, 2020

Completed
11 months until next milestone

Study Start

First participant enrolled

August 21, 2021

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 21, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 20, 2026

Last Updated

August 19, 2022

Status Verified

August 1, 2022

Enrollment Period

5 years

First QC Date

October 1, 2020

Last Update Submit

August 17, 2022

Conditions

Keywords

alcohol

Outcome Measures

Primary Outcomes (5)

  • Detection of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use Using the RAPS4-QF Instrument

    Following the RAPS4-QF screening by AAPL, we anticipate that we will detect a 30% detection of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use.

    15 minutes

  • Detection of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use based on adverse life experiences Using the RAPS4-QF Instrument

    Following the RAPS4-QF screening by AAPL, we anticipate that AAPLs with adverse life experiences will have a 40% detection rate of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use.

    15 minutes

  • Detection of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use based on Race/Ethnicity Using the RAPS4-QF Instrument

    Following the RAPS4-QF screening by AAPL, we anticipate that AAPLs with matching race/ethnicity will have a 30% detection rate of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use.

    15 minutes

  • Detection of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use based on drinking status Using the RAPS4-QF Instrument

    Following the RAPS4-QF screening by AAPL, we anticipate that AAPLs that are alcohol non-abstainers will have a 30% detection rate of problematic alcohol use (i.e. HED or AUD) and at-risk alcohol use.

    15 minutes

  • Percentage of Participants Achieving Decreased Levels of Alcohol Risk Using the SBIRT Intervention

    By comparison of pre-, post- intervention, and six-months follow-up data, we anticipate the following compared to baseline: a 30% change in alcohol risk.

    Intervention: 15 minutes; Follow-up Point: 6 months post-intervention

Study Arms (1)

Screening and Brief Intervention of Problematic Alcohol Use

EXPERIMENTAL

We plan to test the feasibility and effectiveness of the delivery of the peer-based SBIRT using the RAPS4-QF screening tool with CDU students. Furthermore, we will compare delivery by AAPLs' race/ethnicity, drinking status (abstainer vs. non-abstainer), and adverse life experiences. Following the screening by AAPLs, we expect a 30% detection of problematic alcohol use (i.e. high episodic drinking \[HED\] or AUD) and at-risk alcohol use. Participants that screen positive will receive brief motivational interviewing and referral to treatment and will be contacted 6 months following the SBIRT to assess their drinking behaviors. We expect that participants will decrease their alcohol consumption or drinking risk at the 6-month follow up.

Behavioral: Screening and Brief Intervention of Problematic Alcohol Use

Interventions

Provide/enhance knowledge, screening and detection, modify attitudes, motivate and provide skills and resources to reduce alcohol related risk and consumption.

Screening and Brief Intervention of Problematic Alcohol Use

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • enrolled student at CDU
  • age 18 or older
  • Speak and understand English

You may not qualify if:

  • not enrolled as a student at CDU
  • Under the age of 18
  • Unable to speak English

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

AlcoholismAlcohol DrinkingAlcohol-Related Disorders

Interventions

Mass ScreeningEthanol

Condition Hierarchy (Ancestors)

Substance-Related DisordersChemically-Induced DisordersMental DisordersDrinking BehaviorBehavior

Intervention Hierarchy (Ancestors)

Diagnostic Techniques and ProceduresDiagnosisHealth SurveysSurveys and QuestionnairesData CollectionEpidemiologic MethodsInvestigative TechniquesDiagnostic ServicesPreventive Health ServicesHealth ServicesHealth Care Facilities Workforce and ServicesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public HealthPublic Health PracticeAlcoholsOrganic Chemicals

Study Officials

  • Sharon Cobb, PhD

    Charles R. Drew University of Medicine & Science

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 1, 2020

First Posted

October 8, 2020

Study Start

August 21, 2021

Primary Completion (Estimated)

August 21, 2026

Study Completion (Estimated)

October 20, 2026

Last Updated

August 19, 2022

Record last verified: 2022-08