NCT07475988

Brief Summary

Together, alcohol use and suicide account for approximately 4 million deaths per year, with a considerable burden on low and middle-income countries. Tanzania is among the world's most underserved nations for mental health treatment, with very little capacity to treat suicidality or alcohol use disorders. In this study, the researchers will adapt an evidence-based intervention for suicide prevention to address the unique needs of people with alcohol use disorders in Tanzania, and rigorously pilot test the intervention to assess its feasibility and acceptability in a Tanzanian emergency department.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
19mo left

Started Aug 2027

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 12, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 17, 2026

Completed
1.4 years until next milestone

Study Start

First participant enrolled

August 1, 2027

Expected
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2029

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2029

Last Updated

March 17, 2026

Status Verified

March 1, 2026

Enrollment Period

1.6 years

First QC Date

March 12, 2026

Last Update Submit

March 12, 2026

Conditions

Keywords

TelehealthNurse-delivered interventionsStigma reductionCare engagementSuicide preventionHealth behaviorAlcohol use disorderHarm reduction

Outcome Measures

Primary Outcomes (5)

  • Acceptability of intervention

    Acceptability of Intervention Measure (AIM). Four items scored from 1-Completely disagree to 5-Completely agree. Scores are summed for a total score of 4 to 20, with higher scores indicating greater acceptability.

    3 months

  • Enrollment feasibility as measured by the percentage of ED patients with documented screening for study eligibility

    up to 1 year

  • Enrollment feasibility as measured by the number of eligible participants who declined enrollment

    up to 1 year

  • Enrollment feasibility as measured by the time needed to enroll 30 eligible participants

    up to 1 year

  • Retention feasibility as measured by the number of participants retained for follow-up

    session 2 (2 weeks), session 3 (4 weeks), and 3 months

Study Arms (1)

IDEAS-AUD

EXPERIMENTAL

3 sessions of telehealth-delivered counseling

Behavioral: IDEAS-AUD

Interventions

IDEAS-AUDBEHAVIORAL

Telehealth-delivered counseling to reduce suicide risk among people with Alcohol Use Disorder (AUD) who are presenting for care in the KCMC Emergency Department (ED).

IDEAS-AUD

Eligibility Criteria

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

You may qualify if:

  • years of age or older
  • screen positive for alcohol use disorder (AUDIT \>=8)
  • have had suicidal thinking (C-SSRS item indicating "actual thoughts of suicide") in last 30 days
  • clinically sober
  • medically stable
  • have the physical and cognitive capacity to provide consent and complete study procedures
  • able to communicate in Swahili or English

You may not qualify if:

  • prisoners
  • decline or unable to complete informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

AlcoholismSuicide PreventionHealth BehaviorHarm Reduction

Condition Hierarchy (Ancestors)

Alcohol-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental DisordersSuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Brandon Knettel, PhD

    Duke University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Brandon Knettel, PhD

CONTACT

Study Design

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

Study Record Dates

First Submitted

March 12, 2026

First Posted

March 17, 2026

Study Start (Estimated)

August 1, 2027

Primary Completion (Estimated)

March 1, 2029

Study Completion (Estimated)

March 1, 2029

Last Updated

March 17, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will share